Canonical Allele Identifier: CA1624303376

Gene: GNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960858_42960859delinsTG , CM000668.2:g.42960858_42960859delinsTG	GRCh38
NC_000006.11:g.42928596_42928597delinsTG , CM000668.1:g.42928596_42928597delinsTG	GRCh37
NC_000006.10:g.43036574_43036575delinsTG	NCBI36
NG_008396.1:g.5097_5098delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.91_92delinsTG MANE Select	ENSP00000361894.3:p.Trp31=
ENST00000372808.3:c.91_92delinsTG	ENSP00000361894.3:p.Trp31=
NM_018960.4:c.91_92delinsTG	NP_061833.1:p.Trp31=
XM_011514493.1:c.-13-1354_-13-1353delinsTG	XP_011512795.1:n.-13-1354_-13-1353delinsTG
XM_011514494.1:c.-13-1354_-13-1353delinsTG	XP_011512796.1:n.-13-1354_-13-1353delinsTG
NM_001318856.1:c.9-1354_9-1353delinsTG	NP_001305785.1:n.9-1354_9-1353delinsTG
NM_001318857.1:c.152-1904_152-1903delinsTG	NP_001305786.1:n.152-1904_152-1903delinsTG
NM_001318858.1:c.152-1904_152-1903delinsTG	NP_001305787.1:n.152-1904_152-1903delinsTG
NM_001318865.1:c.91_92delinsTG	NP_001305794.1:p.Trp31=
NM_018960.5:c.91_92delinsTG	NP_061833.1:p.Trp31=
NR_134890.1:n.690-1904_690-1903delinsTG
NR_134891.1:n.593-1904_593-1903delinsTG
NR_134892.1:n.593-1354_593-1353delinsTG
NR_134899.1:n.105_106delinsTG
NM_018960.6:c.91_92delinsTG MANE Select	NP_061833.1:p.Trp31=
NM_001318856.2:c.9-1354_9-1353delinsTG	NP_001305785.1:n.9-1354_9-1353delinsTG
NM_001318857.2:c.152-1904_152-1903delinsTG	NP_001305786.1:n.152-1904_152-1903delinsTG
NM_001318858.2:c.152-1904_152-1903delinsTG	NP_001305787.1:n.152-1904_152-1903delinsTG
NM_001318865.2:c.91_92delinsTG	NP_001305794.1:p.Trp31=
NR_134890.2:n.340-1904_340-1903delinsTG
NR_134891.2:n.243-1904_243-1903delinsTG
NR_134892.2:n.243-1354_243-1353delinsTG
NR_134899.2:n.105_106delinsTG