Canonical Allele Identifier: CA1941467520
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472339C= , CM000672.2:g.122472339C= GRCh38
NC_000010.10:g.124231855C= , CM000672.1:g.124231855C= GRCh37
NC_000010.9:g.124221845C= NCBI36
NG_011554.1:g.15815C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10215C= MANE Select ENSP00000357980.3:n.472+10215C=
ENST00000648167.1:c.154+13630C= ENSP00000498033.1:n.154+13630C=
ENST00000368984.7:c.472+10215C= ENSP00000357980.3:n.472+10215C=
NM_002775.4:c.472+10215C= NP_002766.1:n.472+10215C=
NM_002775.5:c.472+10215C= MANE Select NP_002766.1:n.472+10215C=
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