Canonical Allele Identifier: CA1291842308

Gene: HNMT

Linked Data

• dbSNP Id: rs1680715504

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.137988417del , CM000664.2:g.137988417del	GRCh38
NC_000002.11:g.138745987del , CM000664.1:g.138745987del	GRCh37
NC_000002.10:g.138462457del	NCBI36
NG_012966.1:g.29180del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280097.5:c.191-12501del MANE Select	ENSP00000280097.3:n.191-12501del
ENST00000280097.4:c.191-12501del	ENSP00000280097.3:n.191-12501del
ENST00000410115.5:c.191-12501del	ENSP00000386940.1:n.191-12501del
ENST00000467390.5:n.203-12501del
ENST00000475675.5:c.*456-3399del	ENSP00000419415.1:n.*456-3399del
ENST00000480534.1:n.169-148del
ENST00000485653.1:n.123-12501del
NM_006895.2:c.191-12501del	NP_008826.1:n.191-12501del
XM_011511063.1:c.89-12501del	XP_011509365.1:n.89-12501del
XM_011511064.1:c.-188-12501del	XP_011509366.1:n.-188-12501del
XM_011511064.2:c.-188-12501del	XP_011509366.1:n.-188-12501del
XM_017003948.1:c.89-12501del	XP_016859437.1:n.89-12501del
XM_017003949.2:c.191-12501del	XP_016859438.1:n.191-12501del
XR_001739719.1:n.1040-7737del
XR_002959286.1:n.578-12501del
NM_006895.3:c.191-12501del MANE Select	NP_008826.1:n.191-12501del