Canonical Allele Identifier: CA2581810161

Gene: HNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138014190A>T , CM000664.2:g.138014190A>T	GRCh38
NC_000002.11:g.138771760A>T , CM000664.1:g.138771760A>T	GRCh37
NC_000002.10:g.138488230A>T	NCBI36
NG_012966.1:g.54953A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280097.5:c.*60A>T MANE Select	ENSP00000280097.3:n.*60A>T
ENST00000280097.4:c.*60A>T	ENSP00000280097.3:n.*60A>T
ENST00000410115.5:c.*60A>T	ENSP00000386940.1:n.*60A>T
NM_006895.2:c.*60A>T	NP_008826.1:n.*60A>T
XM_011511063.1:c.*60A>T	XP_011509365.1:n.*60A>T
XM_011511064.1:c.*60A>T	XP_011509366.1:n.*60A>T
XM_011511064.2:c.*60A>T	XP_011509366.1:n.*60A>T
XM_017003948.1:c.*60A>T	XP_016859437.1:n.*60A>T
XR_001739719.1:n.232-6394T>A
XR_002959286.1:n.1326A>T
NM_006895.3:c.*60A>T MANE Select	NP_008826.1:n.*60A>T