Canonical Allele Identifier: CA1941477418

Gene: HTRA1

Linked Data

• dbSNP Id: rs762172527

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122507202_122507204del , CM000672.2:g.122507202_122507204del	GRCh38
NC_000010.10:g.124266718_124266720del , CM000672.1:g.124266718_124266720del	GRCh37
NC_000010.9:g.124256708_124256710del	NCBI36
NG_011554.1:g.50678_50680del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.973-168_973-166del MANE Select	ENSP00000357980.3:n.973-168_973-166del
ENST00000648167.1:c.655-168_655-166del	ENSP00000498033.1:n.655-168_655-166del
ENST00000368984.7:c.973-168_973-166del	ENSP00000357980.3:n.973-168_973-166del
ENST00000420892.1:c.196-168_196-166del	ENSP00000412676.1:n.196-168_196-166del
NM_002775.4:c.973-168_973-166del	NP_002766.1:n.973-168_973-166del
NM_002775.5:c.973-168_973-166del MANE Select	NP_002766.1:n.973-168_973-166del