Canonical Allele Identifier: CA384357269

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32731031T>C , CM000674.2:g.32731031T>C GRCh38
NC_000012.11:g.32883965T>C , CM000674.1:g.32883965T>C GRCh37
NC_000012.10:g.32775232T>C NCBI36
NG_012219.1:g.56829T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000434676.7:c.*463T>C (DNM1L) ENSP00000390090.2:n.*463T>C
ENST00000546757.6:c.*783T>C (DNM1L) ENSP00000448105.2:n.*783T>C
ENST00000547078.6:c.1136T>C (DNM1L) ENSP00000448802.2:p.Ile379Thr
ENST00000547719.2:n.2730T>C (DNM1L)
ENST00000547932.6:c.*463T>C (DNM1L) ENSP00000515272.1:n.*463T>C
ENST00000548671.6:c.*644T>C (DNM1L) ENSP00000515271.1:n.*644T>C
ENST00000548750.6:c.1010T>C (DNM1L) ENSP00000447788.2:p.Ile337Thr
ENST00000549926.6:c.650T>C (DNM1L) ENSP00000515263.1:p.Ile217Thr
ENST00000550011.6:c.*1087T>C (DNM1L) ENSP00000515261.1:n.*1087T>C
ENST00000550093.6:n.1184T>C (DNM1L)
ENST00000551076.6:c.*714T>C (DNM1L) ENSP00000515275.1:n.*714T>C
ENST00000551476.6:c.1046T>C (DNM1L) ENSP00000447845.2:p.Ile349Thr
ENST00000551643.6:c.*928T>C (DNM1L) ENSP00000450401.1:n.*928T>C
ENST00000703337.1:c.*894T>C (DNM1L) ENSP00000515262.1:n.*894T>C
ENST00000703338.1:c.650T>C (DNM1L) ENSP00000515264.1:p.Ile217Thr
ENST00000703360.1:c.*783T>C (DNM1L) ENSP00000515270.1:n.*783T>C
ENST00000703361.1:c.728T>C (DNM1L) ENSP00000515273.1:p.Ile243Thr
ENST00000703362.1:c.*463T>C (DNM1L) ENSP00000515274.1:n.*463T>C
ENST00000703363.1:n.2718T>C (DNM1L)
ENST00000703364.1:n.2795T>C (DNM1L)
ENST00000703365.1:c.1123T>C (DNM1L) ENSP00000515276.1:p.Phe375Leu
ENST00000703366.1:n.2157T>C (DNM1L)
ENST00000703367.1:c.1097T>C (DNM1L) ENSP00000515277.1:p.Ile366Thr
ENST00000703368.1:c.*644T>C (DNM1L) ENSP00000515278.1:n.*644T>C
ENST00000703369.1:c.728T>C (DNM1L) ENSP00000515279.1:p.Ile243Thr
ENST00000703370.1:c.650T>C (DNM1L) ENSP00000515280.1:p.Ile217Thr
ENST00000703371.1:c.650T>C (DNM1L) ENSP00000515281.1:p.Ile217Thr
ENST00000703372.1:c.890T>C (DNM1L) ENSP00000515282.1:p.Ile297Thr
ENST00000549701.6:c.1097T>C (DNM1L) MANE Select ENSP00000450399.1:p.Ile366Thr
ENST00000553257.6:c.1136T>C (DNM1L) MANE Plus Clinical ENSP00000449089.1:p.Ile379Thr
ENST00000266481.10:c.1097T>C (DNM1L) ENSP00000266481.6:p.Ile366Thr
ENST00000358214.9:c.1136T>C (DNM1L) ENSP00000350948.5:p.Ile379Thr
ENST00000381000.8:c.1136T>C (DNM1L) ENSP00000370388.4:p.Ile379Thr
ENST00000413295.6:c.*346T>C (DNM1L) ENSP00000396030.2:n.*346T>C
ENST00000414834.6:c.488T>C (DNM1L) ENSP00000404160.2:p.Ile163Thr
ENST00000434676.6:c.*463T>C (DNM1L) ENSP00000390090.2:n.*463T>C
ENST00000452533.6:c.1097T>C (DNM1L) ENSP00000415131.2:p.Ile366Thr
ENST00000546649.5:c.*339T>C (DNM1L) ENSP00000448936.1:n.*339T>C
ENST00000546757.5:c.948T>C (DNM1L) ENSP00000448105.1:n.948T>C
ENST00000547312.5:c.1097T>C (DNM1L) ENSP00000448610.1:p.Ile366Thr
ENST00000549701.5:c.1097T>C (DNM1L) ENSP00000450399.1:p.Ile366Thr
ENST00000551673.5:n.460-3512A>G (YARS2)
ENST00000553257.5:c.1136T>C (DNM1L) ENSP00000449089.1:p.Ile379Thr
NM_001278463.1:c.1097T>C (DNM1L) NP_001265392.1:p.Ile366Thr
NM_001278464.1:c.1136T>C (DNM1L) NP_001265393.1:p.Ile379Thr
NM_001278465.1:c.1136T>C (DNM1L) NP_001265394.1:p.Ile379Thr
NM_001278466.1:c.488T>C (DNM1L) NP_001265395.1:p.Ile163Thr
NM_005690.4:c.1097T>C (DNM1L) NP_005681.2:p.Ile366Thr
NM_012062.4:c.1097T>C (DNM1L) NP_036192.2:p.Ile366Thr
NM_012063.3:c.1097T>C (DNM1L) NP_036193.2:p.Ile366Thr
XM_005253282.3:c.1136T>C (DNM1L) XP_005253339.1:p.Ile379Thr
XM_005253283.3:c.650T>C (DNM1L) XP_005253340.1:p.Ile217Thr
XM_011520543.1:c.1136T>C (DNM1L) XP_011518845.1:p.Ile379Thr
XM_011520544.1:c.440T>C (DNM1L) XP_011518846.1:p.Ile147Thr
XR_242891.3:n.1832+601A>G (YARS2)
XR_242892.3:n.1650-5666A>G (YARS2)
XR_429036.1:n.1707+601A>G (YARS2)
XR_931297.1:n.1832+601A>G (YARS2)
XR_931298.1:n.1707+601A>G (YARS2)
XR_931299.1:n.1650-3512A>G (YARS2)
NM_001330380.1:c.1136T>C (DNM1L) NP_001317309.1:p.Ile379Thr
XM_011520543.3:c.1136T>C (DNM1L) XP_011518845.1:p.Ile379Thr
XM_011520544.2:c.440T>C (DNM1L) XP_011518846.1:p.Ile147Thr
XM_017018663.2:c.440T>C (DNM1L) XP_016874152.1:p.Ile147Thr
XM_017018664.1:c.440T>C (DNM1L) XP_016874153.1:p.Ile147Thr
XM_017018665.1:c.440T>C (DNM1L) XP_016874154.1:p.Ile147Thr
XR_001748730.2:n.2272-5666A>G (YARS2)
XR_002957331.1:n.2147-3512A>G (YARS2)
XR_242892.5:n.2147-5666A>G (YARS2)
NM_012062.5:c.1097T>C (DNM1L) MANE Select NP_036192.2:p.Ile366Thr
NM_001278463.2:c.1097T>C (DNM1L) NP_001265392.1:p.Ile366Thr
NM_001278464.2:c.1136T>C (DNM1L) MANE Plus Clinical NP_001265393.1:p.Ile379Thr
NM_001278465.2:c.1136T>C (DNM1L) NP_001265394.1:p.Ile379Thr
NM_001278466.2:c.488T>C (DNM1L) NP_001265395.1:p.Ile163Thr
NM_001330380.2:c.1136T>C (DNM1L) NP_001317309.1:p.Ile379Thr
NM_005690.5:c.1097T>C (DNM1L) NP_005681.2:p.Ile366Thr
NM_012063.4:c.1097T>C (DNM1L) NP_036193.2:p.Ile366Thr