Canonical Allele Identifier: CA1941477435
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122507263C= , CM000672.2:g.122507263C= GRCh38
NC_000010.10:g.124266779C= , CM000672.1:g.124266779C= GRCh37
NC_000010.9:g.124256769C= NCBI36
NG_011554.1:g.50739C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.973-107C= MANE Select ENSP00000357980.3:n.973-107C=
ENST00000648167.1:c.655-107C= ENSP00000498033.1:n.655-107C=
ENST00000368984.7:c.973-107C= ENSP00000357980.3:n.973-107C=
ENST00000420892.1:c.196-107C= ENSP00000412676.1:n.196-107C=
NM_002775.4:c.973-107C= NP_002766.1:n.973-107C=
NM_002775.5:c.973-107C= MANE Select NP_002766.1:n.973-107C=