Canonical Allele Identifier: CA2661302516

Gene: HNMT

Linked Data

• gnomAD v4: 2-138001915-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138001915T>G , CM000664.2:g.138001915T>G	GRCh38
NC_000002.11:g.138759485T>G , CM000664.1:g.138759485T>G	GRCh37
NC_000002.10:g.138475955T>G	NCBI36
NG_012966.1:g.42678T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280097.5:c.299-149T>G MANE Select	ENSP00000280097.3:n.299-149T>G
ENST00000280097.4:c.299-149T>G	ENSP00000280097.3:n.299-149T>G
ENST00000410115.5:c.299-149T>G	ENSP00000386940.1:n.299-149T>G
ENST00000467390.5:n.311-149T>G
ENST00000485653.1:n.231-149T>G
NM_006895.2:c.299-149T>G	NP_008826.1:n.299-149T>G
XM_011511063.1:c.197-149T>G	XP_011509365.1:n.197-149T>G
XM_011511064.1:c.-80-149T>G	XP_011509366.1:n.-80-149T>G
XM_011511064.2:c.-80-149T>G	XP_011509366.1:n.-80-149T>G
XM_017003948.1:c.197-149T>G	XP_016859437.1:n.197-149T>G
XM_017003949.2:c.299-149T>G	XP_016859438.1:n.299-149T>G
XR_001739719.1:n.1039+5074A>C
XR_002959286.1:n.686-149T>G
NM_006895.3:c.299-149T>G MANE Select	NP_008826.1:n.299-149T>G