Canonical Allele Identifier: CA1941477259
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506872A= , CM000672.2:g.122506872A= GRCh38
NC_000010.10:g.124266388A= , CM000672.1:g.124266388A= GRCh37
NC_000010.9:g.124256378A= NCBI36
NG_011554.1:g.50348A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.959A= MANE Select ENSP00000357980.3:p.Asp320=
ENST00000648167.1:c.641A= ENSP00000498033.1:p.Asp214=
ENST00000368984.7:c.959A= ENSP00000357980.3:p.Asp320=
ENST00000420892.1:c.182A= ENSP00000412676.1:p.Asp61=
NM_002775.4:c.959A= NP_002766.1:p.Asp320=
NM_002775.5:c.959A= MANE Select NP_002766.1:p.Asp320=
Search 100 bp 5'
Search 100 bp 3'