Canonical Allele Identifier: CA384357322

Gene: DNM1L YARS2

Linked Data

• MyVariant Identifiers: chr12:g.32883986C>G (hg19) ; chr12:g.32731052C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32731052C>G , CM000674.2:g.32731052C>G	GRCh38
NC_000012.11:g.32883986C>G , CM000674.1:g.32883986C>G	GRCh37
NC_000012.10:g.32775253C>G	NCBI36
NG_012219.1:g.56850C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434676.7:c.*484C>G (DNM1L)	ENSP00000390090.2:n.*484C>G
ENST00000546757.6:c.*804C>G (DNM1L)	ENSP00000448105.2:n.*804C>G
ENST00000547078.6:c.1157C>G (DNM1L)	ENSP00000448802.2:p.Thr386Ser
ENST00000547719.2:n.2751C>G (DNM1L)
ENST00000547932.6:c.*484C>G (DNM1L)	ENSP00000515272.1:n.*484C>G
ENST00000548671.6:c.*665C>G (DNM1L)	ENSP00000515271.1:n.*665C>G
ENST00000548750.6:c.1031C>G (DNM1L)	ENSP00000447788.2:p.Thr344Ser
ENST00000549926.6:c.671C>G (DNM1L)	ENSP00000515263.1:p.Thr224Ser
ENST00000550011.6:c.*1108C>G (DNM1L)	ENSP00000515261.1:n.*1108C>G
ENST00000550093.6:n.1205C>G (DNM1L)
ENST00000551076.6:c.*735C>G (DNM1L)	ENSP00000515275.1:n.*735C>G
ENST00000551476.6:c.1067C>G (DNM1L)	ENSP00000447845.2:p.Thr356Ser
ENST00000551643.6:c.*949C>G (DNM1L)	ENSP00000450401.1:n.*949C>G
ENST00000703337.1:c.*915C>G (DNM1L)	ENSP00000515262.1:n.*915C>G
ENST00000703338.1:c.671C>G (DNM1L)	ENSP00000515264.1:p.Thr224Ser
ENST00000703360.1:c.*804C>G (DNM1L)	ENSP00000515270.1:n.*804C>G
ENST00000703361.1:c.749C>G (DNM1L)	ENSP00000515273.1:p.Thr250Ser
ENST00000703362.1:c.*484C>G (DNM1L)	ENSP00000515274.1:n.*484C>G
ENST00000703363.1:n.2739C>G (DNM1L)
ENST00000703364.1:n.2816C>G (DNM1L)
ENST00000703365.1:c.1144C>G (DNM1L)	ENSP00000515276.1:p.Leu382Val
ENST00000703366.1:n.2178C>G (DNM1L)
ENST00000703367.1:c.1118C>G (DNM1L)	ENSP00000515277.1:p.Thr373Ser
ENST00000703368.1:c.*665C>G (DNM1L)	ENSP00000515278.1:n.*665C>G
ENST00000703369.1:c.749C>G (DNM1L)	ENSP00000515279.1:p.Thr250Ser
ENST00000703370.1:c.671C>G (DNM1L)	ENSP00000515280.1:p.Thr224Ser
ENST00000703371.1:c.671C>G (DNM1L)	ENSP00000515281.1:p.Thr224Ser
ENST00000703372.1:c.911C>G (DNM1L)	ENSP00000515282.1:p.Thr304Ser
ENST00000549701.6:c.1118C>G (DNM1L) MANE Select	ENSP00000450399.1:p.Thr373Ser
ENST00000553257.6:c.1157C>G (DNM1L) MANE Plus Clinical	ENSP00000449089.1:p.Thr386Ser
ENST00000266481.10:c.1118C>G (DNM1L)	ENSP00000266481.6:p.Thr373Ser
ENST00000358214.9:c.1157C>G (DNM1L)	ENSP00000350948.5:p.Thr386Ser
ENST00000381000.8:c.1157C>G (DNM1L)	ENSP00000370388.4:p.Thr386Ser
ENST00000413295.6:c.*367C>G (DNM1L)	ENSP00000396030.2:n.*367C>G
ENST00000414834.6:c.509C>G (DNM1L)	ENSP00000404160.2:p.Thr170Ser
ENST00000434676.6:c.*484C>G (DNM1L)	ENSP00000390090.2:n.*484C>G
ENST00000452533.6:c.1118C>G (DNM1L)	ENSP00000415131.2:p.Thr373Ser
ENST00000546649.5:c.*360C>G (DNM1L)	ENSP00000448936.1:n.*360C>G
ENST00000546757.5:c.969C>G (DNM1L)	ENSP00000448105.1:n.969C>G
ENST00000547312.5:c.1118C>G (DNM1L)	ENSP00000448610.1:p.Thr373Ser
ENST00000549701.5:c.1118C>G (DNM1L)	ENSP00000450399.1:p.Thr373Ser
ENST00000551673.5:n.460-3533G>C (YARS2)
ENST00000553257.5:c.1157C>G (DNM1L)	ENSP00000449089.1:p.Thr386Ser
NM_001278463.1:c.1118C>G (DNM1L)	NP_001265392.1:p.Thr373Ser
NM_001278464.1:c.1157C>G (DNM1L)	NP_001265393.1:p.Thr386Ser
NM_001278465.1:c.1157C>G (DNM1L)	NP_001265394.1:p.Thr386Ser
NM_001278466.1:c.509C>G (DNM1L)	NP_001265395.1:p.Thr170Ser
NM_005690.4:c.1118C>G (DNM1L)	NP_005681.2:p.Thr373Ser
NM_012062.4:c.1118C>G (DNM1L)	NP_036192.2:p.Thr373Ser
NM_012063.3:c.1118C>G (DNM1L)	NP_036193.2:p.Thr373Ser
XM_005253282.3:c.1157C>G (DNM1L)	XP_005253339.1:p.Thr386Ser
XM_005253283.3:c.671C>G (DNM1L)	XP_005253340.1:p.Thr224Ser
XM_011520543.1:c.1157C>G (DNM1L)	XP_011518845.1:p.Thr386Ser
XM_011520544.1:c.461C>G (DNM1L)	XP_011518846.1:p.Thr154Ser
XR_242891.3:n.1832+580G>C (YARS2)
XR_242892.3:n.1650-5687G>C (YARS2)
XR_429036.1:n.1707+580G>C (YARS2)
XR_931297.1:n.1832+580G>C (YARS2)
XR_931298.1:n.1707+580G>C (YARS2)
XR_931299.1:n.1650-3533G>C (YARS2)
NM_001330380.1:c.1157C>G (DNM1L)	NP_001317309.1:p.Thr386Ser
XM_011520543.3:c.1157C>G (DNM1L)	XP_011518845.1:p.Thr386Ser
XM_011520544.2:c.461C>G (DNM1L)	XP_011518846.1:p.Thr154Ser
XM_017018663.2:c.461C>G (DNM1L)	XP_016874152.1:p.Thr154Ser
XM_017018664.1:c.461C>G (DNM1L)	XP_016874153.1:p.Thr154Ser
XM_017018665.1:c.461C>G (DNM1L)	XP_016874154.1:p.Thr154Ser
XR_001748730.2:n.2272-5687G>C (YARS2)
XR_002957331.1:n.2147-3533G>C (YARS2)
XR_242892.5:n.2147-5687G>C (YARS2)
NM_012062.5:c.1118C>G (DNM1L) MANE Select	NP_036192.2:p.Thr373Ser
NM_001278463.2:c.1118C>G (DNM1L)	NP_001265392.1:p.Thr373Ser
NM_001278464.2:c.1157C>G (DNM1L) MANE Plus Clinical	NP_001265393.1:p.Thr386Ser
NM_001278465.2:c.1157C>G (DNM1L)	NP_001265394.1:p.Thr386Ser
NM_001278466.2:c.509C>G (DNM1L)	NP_001265395.1:p.Thr170Ser
NM_001330380.2:c.1157C>G (DNM1L)	NP_001317309.1:p.Thr386Ser
NM_005690.5:c.1118C>G (DNM1L)	NP_005681.2:p.Thr373Ser
NM_012063.4:c.1118C>G (DNM1L)	NP_036193.2:p.Thr373Ser