Canonical Allele Identifier: CA1941460022
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122462091G= , CM000672.2:g.122462091G= GRCh38
NC_000010.10:g.124221607G= , CM000672.1:g.124221607G= GRCh37
NC_000010.9:g.124211597G= NCBI36
NG_011554.1:g.5567G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.439G= MANE Select ENSP00000357980.3:p.Val147=
ENST00000648167.1:c.154+3382G= ENSP00000498033.1:n.154+3382G=
ENST00000368984.7:c.439G= ENSP00000357980.3:p.Val147=
NM_002775.4:c.439G= NP_002766.1:p.Val147=
NM_002775.5:c.439G= MANE Select NP_002766.1:p.Val147=