Canonical Allele Identifier: CA1291857850

Gene: HNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138013774G= , CM000664.2:g.138013774G=	GRCh38
NC_000002.11:g.138771344G= , CM000664.1:g.138771344G=	GRCh37
NC_000002.10:g.138487814G=	NCBI36
NG_012966.1:g.54537G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.524-1G= MANE Select	ENSP00000280097.3:n.524-1G=
ENST00000280097.4:c.524-1G=	ENSP00000280097.3:n.524-1G=
ENST00000410115.5:c.524-1G=	ENSP00000386940.1:n.524-1G=
ENST00000485653.1:n.456-1G=
NM_006895.2:c.524-1G=	NP_008826.1:n.524-1G=
XM_011511063.1:c.422-1G=	XP_011509365.1:n.422-1G=
XM_011511064.1:c.146-1G=	XP_011509366.1:n.146-1G=
XM_011511064.2:c.146-1G=	XP_011509366.1:n.146-1G=
XM_017003948.1:c.422-1G=	XP_016859437.1:n.422-1G=
XR_001739719.1:n.232-5978C=
XR_002959286.1:n.911-1G=
NM_006895.3:c.524-1G= MANE Select	NP_008826.1:n.524-1G=