Canonical Allele Identifier: CA1941477440
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122507267C= , CM000672.2:g.122507267C= GRCh38
NC_000010.10:g.124266783C= , CM000672.1:g.124266783C= GRCh37
NC_000010.9:g.124256773C= NCBI36
NG_011554.1:g.50743C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.973-103C= MANE Select ENSP00000357980.3:n.973-103C=
ENST00000648167.1:c.655-103C= ENSP00000498033.1:n.655-103C=
ENST00000368984.7:c.973-103C= ENSP00000357980.3:n.973-103C=
ENST00000420892.1:c.196-103C= ENSP00000412676.1:n.196-103C=
NM_002775.4:c.973-103C= NP_002766.1:n.973-103C=
NM_002775.5:c.973-103C= MANE Select NP_002766.1:n.973-103C=
Search 100 bp 5'
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