Canonical Allele Identifier: CA384357319

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32731051A>T , CM000674.2:g.32731051A>T GRCh38
NC_000012.11:g.32883985A>T , CM000674.1:g.32883985A>T GRCh37
NC_000012.10:g.32775252A>T NCBI36
NG_012219.1:g.56849A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000434676.7:c.*483A>T (DNM1L) ENSP00000390090.2:n.*483A>T
ENST00000546757.6:c.*803A>T (DNM1L) ENSP00000448105.2:n.*803A>T
ENST00000547078.6:c.1156A>T (DNM1L) ENSP00000448802.2:p.Thr386Ser
ENST00000547719.2:n.2750A>T (DNM1L)
ENST00000547932.6:c.*483A>T (DNM1L) ENSP00000515272.1:n.*483A>T
ENST00000548671.6:c.*664A>T (DNM1L) ENSP00000515271.1:n.*664A>T
ENST00000548750.6:c.1030A>T (DNM1L) ENSP00000447788.2:p.Thr344Ser
ENST00000549926.6:c.670A>T (DNM1L) ENSP00000515263.1:p.Thr224Ser
ENST00000550011.6:c.*1107A>T (DNM1L) ENSP00000515261.1:n.*1107A>T
ENST00000550093.6:n.1204A>T (DNM1L)
ENST00000551076.6:c.*734A>T (DNM1L) ENSP00000515275.1:n.*734A>T
ENST00000551476.6:c.1066A>T (DNM1L) ENSP00000447845.2:p.Thr356Ser
ENST00000551643.6:c.*948A>T (DNM1L) ENSP00000450401.1:n.*948A>T
ENST00000703337.1:c.*914A>T (DNM1L) ENSP00000515262.1:n.*914A>T
ENST00000703338.1:c.670A>T (DNM1L) ENSP00000515264.1:p.Thr224Ser
ENST00000703360.1:c.*803A>T (DNM1L) ENSP00000515270.1:n.*803A>T
ENST00000703361.1:c.748A>T (DNM1L) ENSP00000515273.1:p.Thr250Ser
ENST00000703362.1:c.*483A>T (DNM1L) ENSP00000515274.1:n.*483A>T
ENST00000703363.1:n.2738A>T (DNM1L)
ENST00000703364.1:n.2815A>T (DNM1L)
ENST00000703365.1:c.1143A>T (DNM1L) ENSP00000515276.1:p.Arg381Ser
ENST00000703366.1:n.2177A>T (DNM1L)
ENST00000703367.1:c.1117A>T (DNM1L) ENSP00000515277.1:p.Thr373Ser
ENST00000703368.1:c.*664A>T (DNM1L) ENSP00000515278.1:n.*664A>T
ENST00000703369.1:c.748A>T (DNM1L) ENSP00000515279.1:p.Thr250Ser
ENST00000703370.1:c.670A>T (DNM1L) ENSP00000515280.1:p.Thr224Ser
ENST00000703371.1:c.670A>T (DNM1L) ENSP00000515281.1:p.Thr224Ser
ENST00000703372.1:c.910A>T (DNM1L) ENSP00000515282.1:p.Thr304Ser
ENST00000549701.6:c.1117A>T (DNM1L) MANE Select ENSP00000450399.1:p.Thr373Ser
ENST00000553257.6:c.1156A>T (DNM1L) MANE Plus Clinical ENSP00000449089.1:p.Thr386Ser
ENST00000266481.10:c.1117A>T (DNM1L) ENSP00000266481.6:p.Thr373Ser
ENST00000358214.9:c.1156A>T (DNM1L) ENSP00000350948.5:p.Thr386Ser
ENST00000381000.8:c.1156A>T (DNM1L) ENSP00000370388.4:p.Thr386Ser
ENST00000413295.6:c.*366A>T (DNM1L) ENSP00000396030.2:n.*366A>T
ENST00000414834.6:c.508A>T (DNM1L) ENSP00000404160.2:p.Thr170Ser
ENST00000434676.6:c.*483A>T (DNM1L) ENSP00000390090.2:n.*483A>T
ENST00000452533.6:c.1117A>T (DNM1L) ENSP00000415131.2:p.Thr373Ser
ENST00000546649.5:c.*359A>T (DNM1L) ENSP00000448936.1:n.*359A>T
ENST00000546757.5:c.968A>T (DNM1L) ENSP00000448105.1:n.968A>T
ENST00000547312.5:c.1117A>T (DNM1L) ENSP00000448610.1:p.Thr373Ser
ENST00000549701.5:c.1117A>T (DNM1L) ENSP00000450399.1:p.Thr373Ser
ENST00000551673.5:n.460-3532T>A (YARS2)
ENST00000553257.5:c.1156A>T (DNM1L) ENSP00000449089.1:p.Thr386Ser
NM_001278463.1:c.1117A>T (DNM1L) NP_001265392.1:p.Thr373Ser
NM_001278464.1:c.1156A>T (DNM1L) NP_001265393.1:p.Thr386Ser
NM_001278465.1:c.1156A>T (DNM1L) NP_001265394.1:p.Thr386Ser
NM_001278466.1:c.508A>T (DNM1L) NP_001265395.1:p.Thr170Ser
NM_005690.4:c.1117A>T (DNM1L) NP_005681.2:p.Thr373Ser
NM_012062.4:c.1117A>T (DNM1L) NP_036192.2:p.Thr373Ser
NM_012063.3:c.1117A>T (DNM1L) NP_036193.2:p.Thr373Ser
XM_005253282.3:c.1156A>T (DNM1L) XP_005253339.1:p.Thr386Ser
XM_005253283.3:c.670A>T (DNM1L) XP_005253340.1:p.Thr224Ser
XM_011520543.1:c.1156A>T (DNM1L) XP_011518845.1:p.Thr386Ser
XM_011520544.1:c.460A>T (DNM1L) XP_011518846.1:p.Thr154Ser
XR_242891.3:n.1832+581T>A (YARS2)
XR_242892.3:n.1650-5686T>A (YARS2)
XR_429036.1:n.1707+581T>A (YARS2)
XR_931297.1:n.1832+581T>A (YARS2)
XR_931298.1:n.1707+581T>A (YARS2)
XR_931299.1:n.1650-3532T>A (YARS2)
NM_001330380.1:c.1156A>T (DNM1L) NP_001317309.1:p.Thr386Ser
XM_011520543.3:c.1156A>T (DNM1L) XP_011518845.1:p.Thr386Ser
XM_011520544.2:c.460A>T (DNM1L) XP_011518846.1:p.Thr154Ser
XM_017018663.2:c.460A>T (DNM1L) XP_016874152.1:p.Thr154Ser
XM_017018664.1:c.460A>T (DNM1L) XP_016874153.1:p.Thr154Ser
XM_017018665.1:c.460A>T (DNM1L) XP_016874154.1:p.Thr154Ser
XR_001748730.2:n.2272-5686T>A (YARS2)
XR_002957331.1:n.2147-3532T>A (YARS2)
XR_242892.5:n.2147-5686T>A (YARS2)
NM_012062.5:c.1117A>T (DNM1L) MANE Select NP_036192.2:p.Thr373Ser
NM_001278463.2:c.1117A>T (DNM1L) NP_001265392.1:p.Thr373Ser
NM_001278464.2:c.1156A>T (DNM1L) MANE Plus Clinical NP_001265393.1:p.Thr386Ser
NM_001278465.2:c.1156A>T (DNM1L) NP_001265394.1:p.Thr386Ser
NM_001278466.2:c.508A>T (DNM1L) NP_001265395.1:p.Thr170Ser
NM_001330380.2:c.1156A>T (DNM1L) NP_001317309.1:p.Thr386Ser
NM_005690.5:c.1117A>T (DNM1L) NP_005681.2:p.Thr373Ser
NM_012063.4:c.1117A>T (DNM1L) NP_036193.2:p.Thr373Ser