Canonical Allele Identifier: CA2661302587

Gene: HNMT

Linked Data

• gnomAD v4: 2-138002021-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138002021G>T , CM000664.2:g.138002021G>T	GRCh38
NC_000002.11:g.138759591G>T , CM000664.1:g.138759591G>T	GRCh37
NC_000002.10:g.138476061G>T	NCBI36
NG_012966.1:g.42784G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280097.5:c.299-43G>T MANE Select	ENSP00000280097.3:n.299-43G>T
ENST00000280097.4:c.299-43G>T	ENSP00000280097.3:n.299-43G>T
ENST00000410115.5:c.299-43G>T	ENSP00000386940.1:n.299-43G>T
ENST00000467390.5:n.311-43G>T
ENST00000485653.1:n.231-43G>T
NM_006895.2:c.299-43G>T	NP_008826.1:n.299-43G>T
XM_011511063.1:c.197-43G>T	XP_011509365.1:n.197-43G>T
XM_011511064.1:c.-80-43G>T	XP_011509366.1:n.-80-43G>T
XM_011511064.2:c.-80-43G>T	XP_011509366.1:n.-80-43G>T
XM_017003948.1:c.197-43G>T	XP_016859437.1:n.197-43G>T
XM_017003949.2:c.299-43G>T	XP_016859438.1:n.299-43G>T
XR_001739719.1:n.1039+4968C>A
XR_002959286.1:n.686-43G>T
NM_006895.3:c.299-43G>T MANE Select	NP_008826.1:n.299-43G>T