Canonical Allele Identifier: CA1291857870

Gene: HNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138013786T= , CM000664.2:g.138013786T=	GRCh38
NC_000002.11:g.138771356T= , CM000664.1:g.138771356T=	GRCh37
NC_000002.10:g.138487826T=	NCBI36
NG_012966.1:g.54549T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.535T= MANE Select	ENSP00000280097.3:p.Trp179=
ENST00000280097.4:c.535T=	ENSP00000280097.3:p.Trp179=
ENST00000410115.5:c.535T=	ENSP00000386940.1:p.Trp179=
ENST00000485653.1:n.467T=
NM_006895.2:c.535T=	NP_008826.1:p.Trp179=
XM_011511063.1:c.433T=	XP_011509365.1:p.Trp145=
XM_011511064.1:c.157T=	XP_011509366.1:p.Trp53=
XM_011511064.2:c.157T=	XP_011509366.1:p.Trp53=
XM_017003948.1:c.433T=	XP_016859437.1:p.Trp145=
XR_001739719.1:n.232-5990A=
XR_002959286.1:n.922T=
NM_006895.3:c.535T= MANE Select	NP_008826.1:p.Trp179=