Canonical Allele Identifier: CA1941467332
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122471960C= , CM000672.2:g.122471960C= GRCh38
NC_000010.10:g.124231476C= , CM000672.1:g.124231476C= GRCh37
NC_000010.9:g.124221466C= NCBI36
NG_011554.1:g.15436C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.472+9836C= MANE Select ENSP00000357980.3:n.472+9836C=
ENST00000648167.1:c.154+13251C= ENSP00000498033.1:n.154+13251C=
ENST00000368984.7:c.472+9836C= ENSP00000357980.3:n.472+9836C=
NM_002775.4:c.472+9836C= NP_002766.1:n.472+9836C=
NM_002775.5:c.472+9836C= MANE Select NP_002766.1:n.472+9836C=
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