Canonical Allele Identifier: CA1941477422
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122507211A= , CM000672.2:g.122507211A= GRCh38
NC_000010.10:g.124266727A= , CM000672.1:g.124266727A= GRCh37
NC_000010.9:g.124256717A= NCBI36
NG_011554.1:g.50687A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.973-159A= MANE Select ENSP00000357980.3:n.973-159A=
ENST00000648167.1:c.655-159A= ENSP00000498033.1:n.655-159A=
ENST00000368984.7:c.973-159A= ENSP00000357980.3:n.973-159A=
ENST00000420892.1:c.196-159A= ENSP00000412676.1:n.196-159A=
NM_002775.4:c.973-159A= NP_002766.1:n.973-159A=
NM_002775.5:c.973-159A= MANE Select NP_002766.1:n.973-159A=
Search 100 bp 5'
Search 100 bp 3'