Canonical Allele Identifier: CA378585549
Gene: HTRA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506772T>G , CM000672.2:g.122506772T>G GRCh38
NC_000010.10:g.124266288T>G , CM000672.1:g.124266288T>G GRCh37
NC_000010.9:g.124256278T>G NCBI36
NG_011554.1:g.50248T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.859T>G MANE Select ENSP00000357980.3:p.Ser287Ala
ENST00000648167.1:c.541T>G ENSP00000498033.1:p.Ser181Ala
ENST00000368984.7:c.859T>G ENSP00000357980.3:p.Ser287Ala
ENST00000420892.1:c.82T>G ENSP00000412676.1:p.Ser28Ala
NM_002775.4:c.859T>G NP_002766.1:p.Ser287Ala
NM_002775.5:c.859T>G MANE Select NP_002766.1:p.Ser287Ala