Canonical Allele Identifier: CA1291848285

Gene: HNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138002099A= , CM000664.2:g.138002099A=	GRCh38
NC_000002.11:g.138759669A= , CM000664.1:g.138759669A=	GRCh37
NC_000002.10:g.138476139A=	NCBI36
NG_012966.1:g.42862A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280097.5:c.334A= MANE Select	ENSP00000280097.3:p.Lys112=
ENST00000280097.4:c.334A=	ENSP00000280097.3:p.Lys112=
ENST00000410115.5:c.334A=	ENSP00000386940.1:p.Lys112=
ENST00000467390.5:n.346A=
ENST00000485653.1:n.266A=
NM_006895.2:c.334A=	NP_008826.1:p.Lys112=
XM_011511063.1:c.232A=	XP_011509365.1:p.Lys78=
XM_011511064.1:c.-45A=	XP_011509366.1:n.-45A=
XM_011511064.2:c.-45A=	XP_011509366.1:n.-45A=
XM_017003948.1:c.232A=	XP_016859437.1:p.Lys78=
XM_017003949.2:c.334A=	XP_016859438.1:p.Lys112=
XR_001739719.1:n.1039+4890T=
XR_002959286.1:n.721A=
NM_006895.3:c.334A= MANE Select	NP_008826.1:p.Lys112=