Canonical Allele Identifier: CA1941477212
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506750G= , CM000672.2:g.122506750G= GRCh38
NC_000010.10:g.124266266G= , CM000672.1:g.124266266G= GRCh37
NC_000010.9:g.124256256G= NCBI36
NG_011554.1:g.50226G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.837G= MANE Select ENSP00000357980.3:p.Val279=
ENST00000648167.1:c.519G= ENSP00000498033.1:p.Val173=
ENST00000368984.7:c.837G= ENSP00000357980.3:p.Val279=
ENST00000420892.1:c.60G= ENSP00000412676.1:p.Val20=
NM_002775.4:c.837G= NP_002766.1:p.Val279=
NM_002775.5:c.837G= MANE Select NP_002766.1:p.Val279=