Canonical Allele Identifier: CA1624303614

Gene: GNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960970C= , CM000668.2:g.42960970C=	GRCh38
NC_000006.11:g.42928708C= , CM000668.1:g.42928708C=	GRCh37
NC_000006.10:g.43036686C=	NCBI36
NG_008396.1:g.5209C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.203C= MANE Select	ENSP00000361894.3:p.Thr68=
ENST00000372808.3:c.203C=	ENSP00000361894.3:p.Thr68=
NM_018960.4:c.203C=	NP_061833.1:p.Thr68=
XM_011514493.1:c.-13-1242C=	XP_011512795.1:n.-13-1242C=
XM_011514494.1:c.-13-1242C=	XP_011512796.1:n.-13-1242C=
NM_001318856.1:c.9-1242C=	NP_001305785.1:n.9-1242C=
NM_001318857.1:c.152-1792C=	NP_001305786.1:n.152-1792C=
NM_001318858.1:c.152-1792C=	NP_001305787.1:n.152-1792C=
NM_001318865.1:c.203C=	NP_001305794.1:p.Thr68=
NM_018960.5:c.203C=	NP_061833.1:p.Thr68=
NR_134890.1:n.690-1792C=
NR_134891.1:n.593-1792C=
NR_134892.1:n.593-1242C=
NR_134899.1:n.217C=
NM_018960.6:c.203C= MANE Select	NP_061833.1:p.Thr68=
NM_001318856.2:c.9-1242C=	NP_001305785.1:n.9-1242C=
NM_001318857.2:c.152-1792C=	NP_001305786.1:n.152-1792C=
NM_001318858.2:c.152-1792C=	NP_001305787.1:n.152-1792C=
NM_001318865.2:c.203C=	NP_001305794.1:p.Thr68=
NR_134890.2:n.340-1792C=
NR_134891.2:n.243-1792C=
NR_134892.2:n.243-1242C=
NR_134899.2:n.217C=