Canonical Allele Identifier: CA1291858013

Gene: HNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138013879A= , CM000664.2:g.138013879A=	GRCh38
NC_000002.11:g.138771449A= , CM000664.1:g.138771449A=	GRCh37
NC_000002.10:g.138487919A=	NCBI36
NG_012966.1:g.54642A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.628A= MANE Select	ENSP00000280097.3:p.Asn210=
ENST00000280097.4:c.628A=	ENSP00000280097.3:p.Asn210=
ENST00000410115.5:c.628A=	ENSP00000386940.1:p.Asn210=
ENST00000485653.1:n.560A=
NM_006895.2:c.628A=	NP_008826.1:p.Asn210=
XM_011511063.1:c.526A=	XP_011509365.1:p.Asn176=
XM_011511064.1:c.250A=	XP_011509366.1:p.Asn84=
XM_011511064.2:c.250A=	XP_011509366.1:p.Asn84=
XM_017003948.1:c.526A=	XP_016859437.1:p.Asn176=
XR_001739719.1:n.232-6083T=
XR_002959286.1:n.1015A=
NM_006895.3:c.628A= MANE Select	NP_008826.1:p.Asn210=