Canonical Allele Identifier: CA428913381

Gene: HNMT

Linked Data

• MyVariant Identifiers: chr2:g.138759671G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138002101G>A , CM000664.2:g.138002101G>A	GRCh38
NC_000002.11:g.138759671G>A , CM000664.1:g.138759671G>A	GRCh37
NC_000002.10:g.138476141G>A	NCBI36
NG_012966.1:g.42864G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.336G>A MANE Select	ENSP00000280097.3:p.Lys112=
ENST00000280097.4:c.336G>A	ENSP00000280097.3:p.Lys112=
ENST00000410115.5:c.336G>A	ENSP00000386940.1:p.Lys112=
ENST00000467390.5:n.348G>A
ENST00000485653.1:n.268G>A
NM_006895.2:c.336G>A	NP_008826.1:p.Lys112=
XM_011511063.1:c.234G>A	XP_011509365.1:p.Lys78=
XM_011511064.1:c.-43G>A	XP_011509366.1:n.-43G>A
XM_011511064.2:c.-43G>A	XP_011509366.1:n.-43G>A
XM_017003948.1:c.234G>A	XP_016859437.1:p.Lys78=
XM_017003949.2:c.336G>A	XP_016859438.1:p.Lys112=
XR_001739719.1:n.1039+4888C>T
XR_002959286.1:n.723G>A
NM_006895.3:c.336G>A MANE Select	NP_008826.1:p.Lys112=