Canonical Allele Identifier: CA1291858021

Gene: HNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138013887G= , CM000664.2:g.138013887G=	GRCh38
NC_000002.11:g.138771457G= , CM000664.1:g.138771457G=	GRCh37
NC_000002.10:g.138487927G=	NCBI36
NG_012966.1:g.54650G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.636G= MANE Select	ENSP00000280097.3:p.Gly212=
ENST00000280097.4:c.636G=	ENSP00000280097.3:p.Gly212=
ENST00000410115.5:c.636G=	ENSP00000386940.1:p.Gly212=
ENST00000485653.1:n.568G=
NM_006895.2:c.636G=	NP_008826.1:p.Gly212=
XM_011511063.1:c.534G=	XP_011509365.1:p.Gly178=
XM_011511064.1:c.258G=	XP_011509366.1:p.Gly86=
XM_011511064.2:c.258G=	XP_011509366.1:p.Gly86=
XM_017003948.1:c.534G=	XP_016859437.1:p.Gly178=
XR_001739719.1:n.232-6091C=
XR_002959286.1:n.1023G=
NM_006895.3:c.636G= MANE Select	NP_008826.1:p.Gly212=