Canonical Allele Identifier: CA1291842311

Gene: HNMT

Linked Data

• dbSNP Id: rs1033173328

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.137988427C>T , CM000664.2:g.137988427C>T	GRCh38
NC_000002.11:g.138745997C>T , CM000664.1:g.138745997C>T	GRCh37
NC_000002.10:g.138462467C>T	NCBI36
NG_012966.1:g.29190C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280097.5:c.191-12491C>T MANE Select	ENSP00000280097.3:n.191-12491C>T
ENST00000280097.4:c.191-12491C>T	ENSP00000280097.3:n.191-12491C>T
ENST00000410115.5:c.191-12491C>T	ENSP00000386940.1:n.191-12491C>T
ENST00000467390.5:n.203-12491C>T
ENST00000475675.5:c.*456-3389C>T	ENSP00000419415.1:n.*456-3389C>T
ENST00000480534.1:n.169-138C>T
ENST00000485653.1:n.123-12491C>T
NM_006895.2:c.191-12491C>T	NP_008826.1:n.191-12491C>T
XM_011511063.1:c.89-12491C>T	XP_011509365.1:n.89-12491C>T
XM_011511064.1:c.-188-12491C>T	XP_011509366.1:n.-188-12491C>T
XM_011511064.2:c.-188-12491C>T	XP_011509366.1:n.-188-12491C>T
XM_017003948.1:c.89-12491C>T	XP_016859437.1:n.89-12491C>T
XM_017003949.2:c.191-12491C>T	XP_016859438.1:n.191-12491C>T
XR_001739719.1:n.1040-7748G>A
XR_002959286.1:n.578-12491C>T
NM_006895.3:c.191-12491C>T MANE Select	NP_008826.1:n.191-12491C>T