Canonical Allele Identifier: CA1941477223
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506763A= , CM000672.2:g.122506763A= GRCh38
NC_000010.10:g.124266279A= , CM000672.1:g.124266279A= GRCh37
NC_000010.9:g.124256269A= NCBI36
NG_011554.1:g.50239A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.850A= MANE Select ENSP00000357980.3:p.Ser284=
ENST00000648167.1:c.532A= ENSP00000498033.1:p.Ser178=
ENST00000368984.7:c.850A= ENSP00000357980.3:p.Ser284=
ENST00000420892.1:c.73A= ENSP00000412676.1:p.Ser25=
NM_002775.4:c.850A= NP_002766.1:p.Ser284=
NM_002775.5:c.850A= MANE Select NP_002766.1:p.Ser284=
Search 100 bp 5'
Search 100 bp 3'