Canonical Allele Identifier: CA1941477135
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506580G= , CM000672.2:g.122506580G= GRCh38
NC_000010.10:g.124266096G= , CM000672.1:g.124266096G= GRCh37
NC_000010.9:g.124256086G= NCBI36
NG_011554.1:g.50056G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.778-111G= MANE Select ENSP00000357980.3:n.778-111G=
ENST00000648167.1:c.460-111G= ENSP00000498033.1:n.460-111G=
ENST00000368984.7:c.778-111G= ENSP00000357980.3:n.778-111G=
NM_002775.4:c.778-111G= NP_002766.1:n.778-111G=
NM_002775.5:c.778-111G= MANE Select NP_002766.1:n.778-111G=
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