Canonical Allele Identifier: CA1291857867

Gene: HNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138013785C= , CM000664.2:g.138013785C=	GRCh38
NC_000002.11:g.138771355C= , CM000664.1:g.138771355C=	GRCh37
NC_000002.10:g.138487825C=	NCBI36
NG_012966.1:g.54548C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.534C= MANE Select	ENSP00000280097.3:p.Gly178=
ENST00000280097.4:c.534C=	ENSP00000280097.3:p.Gly178=
ENST00000410115.5:c.534C=	ENSP00000386940.1:p.Gly178=
ENST00000485653.1:n.466C=
NM_006895.2:c.534C=	NP_008826.1:p.Gly178=
XM_011511063.1:c.432C=	XP_011509365.1:p.Gly144=
XM_011511064.1:c.156C=	XP_011509366.1:p.Gly52=
XM_011511064.2:c.156C=	XP_011509366.1:p.Gly52=
XM_017003948.1:c.432C=	XP_016859437.1:p.Gly144=
XR_001739719.1:n.232-5989G=
XR_002959286.1:n.921C=
NM_006895.3:c.534C= MANE Select	NP_008826.1:p.Gly178=