Canonical Allele Identifier: CA1941477238
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506813C= , CM000672.2:g.122506813C= GRCh38
NC_000010.10:g.124266329C= , CM000672.1:g.124266329C= GRCh37
NC_000010.9:g.124256319C= NCBI36
NG_011554.1:g.50289C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.900C= MANE Select ENSP00000357980.3:p.Thr300=
ENST00000648167.1:c.582C= ENSP00000498033.1:p.Thr194=
ENST00000368984.7:c.900C= ENSP00000357980.3:p.Thr300=
ENST00000420892.1:c.123C= ENSP00000412676.1:p.Thr41=
NM_002775.4:c.900C= NP_002766.1:p.Thr300=
NM_002775.5:c.900C= MANE Select NP_002766.1:p.Thr300=
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