Canonical Allele Identifier: CA1291858005

Gene: HNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138013874T= , CM000664.2:g.138013874T=	GRCh38
NC_000002.11:g.138771444T= , CM000664.1:g.138771444T=	GRCh37
NC_000002.10:g.138487914T=	NCBI36
NG_012966.1:g.54637T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.623T= MANE Select	ENSP00000280097.3:p.Leu208=
ENST00000280097.4:c.623T=	ENSP00000280097.3:p.Leu208=
ENST00000410115.5:c.623T=	ENSP00000386940.1:p.Leu208=
ENST00000485653.1:n.555T=
NM_006895.2:c.623T=	NP_008826.1:p.Leu208=
XM_011511063.1:c.521T=	XP_011509365.1:p.Leu174=
XM_011511064.1:c.245T=	XP_011509366.1:p.Leu82=
XM_011511064.2:c.245T=	XP_011509366.1:p.Leu82=
XM_017003948.1:c.521T=	XP_016859437.1:p.Leu174=
XR_001739719.1:n.232-6078A=
XR_002959286.1:n.1010T=
NM_006895.3:c.623T= MANE Select	NP_008826.1:p.Leu208=