Canonical Allele Identifier: CA2577113611

Gene: HNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138001998A>C , CM000664.2:g.138001998A>C	GRCh38
NC_000002.11:g.138759568A>C , CM000664.1:g.138759568A>C	GRCh37
NC_000002.10:g.138476038A>C	NCBI36
NG_012966.1:g.42761A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.299-66A>C MANE Select	ENSP00000280097.3:n.299-66A>C
ENST00000280097.4:c.299-66A>C	ENSP00000280097.3:n.299-66A>C
ENST00000410115.5:c.299-66A>C	ENSP00000386940.1:n.299-66A>C
ENST00000467390.5:n.311-66A>C
ENST00000485653.1:n.231-66A>C
NM_006895.2:c.299-66A>C	NP_008826.1:n.299-66A>C
XM_011511063.1:c.197-66A>C	XP_011509365.1:n.197-66A>C
XM_011511064.1:c.-80-66A>C	XP_011509366.1:n.-80-66A>C
XM_011511064.2:c.-80-66A>C	XP_011509366.1:n.-80-66A>C
XM_017003948.1:c.197-66A>C	XP_016859437.1:n.197-66A>C
XM_017003949.2:c.299-66A>C	XP_016859438.1:n.299-66A>C
XR_001739719.1:n.1039+4991T>G
XR_002959286.1:n.686-66A>C
NM_006895.3:c.299-66A>C MANE Select	NP_008826.1:n.299-66A>C