Canonical Allele Identifier: CA1291848216

Gene: HNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138001929T= , CM000664.2:g.138001929T=	GRCh38
NC_000002.11:g.138759499T= , CM000664.1:g.138759499T=	GRCh37
NC_000002.10:g.138475969T=	NCBI36
NG_012966.1:g.42692T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.299-135T= MANE Select	ENSP00000280097.3:n.299-135T=
ENST00000280097.4:c.299-135T=	ENSP00000280097.3:n.299-135T=
ENST00000410115.5:c.299-135T=	ENSP00000386940.1:n.299-135T=
ENST00000467390.5:n.311-135T=
ENST00000485653.1:n.231-135T=
NM_006895.2:c.299-135T=	NP_008826.1:n.299-135T=
XM_011511063.1:c.197-135T=	XP_011509365.1:n.197-135T=
XM_011511064.1:c.-80-135T=	XP_011509366.1:n.-80-135T=
XM_011511064.2:c.-80-135T=	XP_011509366.1:n.-80-135T=
XM_017003948.1:c.197-135T=	XP_016859437.1:n.197-135T=
XM_017003949.2:c.299-135T=	XP_016859438.1:n.299-135T=
XR_001739719.1:n.1039+5060A=
XR_002959286.1:n.686-135T=
NM_006895.3:c.299-135T= MANE Select	NP_008826.1:n.299-135T=