Canonical Allele Identifier: CA1624303568

Gene: GNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960950_42960952delinsGCT , CM000668.2:g.42960950_42960952delinsGCT	GRCh38
NC_000006.11:g.42928688_42928690delinsGCT , CM000668.1:g.42928688_42928690delinsGCT	GRCh37
NC_000006.10:g.43036666_43036668delinsGCT	NCBI36
NG_008396.1:g.5189_5191delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.183_185delinsGCT MANE Select	ENSP00000361894.3:p.Val61=
ENST00000372808.3:c.183_185delinsGCT	ENSP00000361894.3:p.Val61=
NM_018960.4:c.183_185delinsGCT	NP_061833.1:p.Val61=
XM_011514493.1:c.-13-1262_-13-1260delinsGCT	XP_011512795.1:n.-13-1262_-13-1260delinsGCT
XM_011514494.1:c.-13-1262_-13-1260delinsGCT	XP_011512796.1:n.-13-1262_-13-1260delinsGCT
NM_001318856.1:c.9-1262_9-1260delinsGCT	NP_001305785.1:n.9-1262_9-1260delinsGCT
NM_001318857.1:c.152-1812_152-1810delinsGCT	NP_001305786.1:n.152-1812_152-1810delinsGCT
NM_001318858.1:c.152-1812_152-1810delinsGCT	NP_001305787.1:n.152-1812_152-1810delinsGCT
NM_001318865.1:c.183_185delinsGCT	NP_001305794.1:p.Val61=
NM_018960.5:c.183_185delinsGCT	NP_061833.1:p.Val61=
NR_134890.1:n.690-1812_690-1810delinsGCT
NR_134891.1:n.593-1812_593-1810delinsGCT
NR_134892.1:n.593-1262_593-1260delinsGCT
NR_134899.1:n.197_199delinsGCT
NM_018960.6:c.183_185delinsGCT MANE Select	NP_061833.1:p.Val61=
NM_001318856.2:c.9-1262_9-1260delinsGCT	NP_001305785.1:n.9-1262_9-1260delinsGCT
NM_001318857.2:c.152-1812_152-1810delinsGCT	NP_001305786.1:n.152-1812_152-1810delinsGCT
NM_001318858.2:c.152-1812_152-1810delinsGCT	NP_001305787.1:n.152-1812_152-1810delinsGCT
NM_001318865.2:c.183_185delinsGCT	NP_001305794.1:p.Val61=
NR_134890.2:n.340-1812_340-1810delinsGCT
NR_134891.2:n.243-1812_243-1810delinsGCT
NR_134892.2:n.243-1262_243-1260delinsGCT
NR_134899.2:n.197_199delinsGCT