Canonical Allele Identifier: CA1941477134
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506579G= , CM000672.2:g.122506579G= GRCh38
NC_000010.10:g.124266095G= , CM000672.1:g.124266095G= GRCh37
NC_000010.9:g.124256085G= NCBI36
NG_011554.1:g.50055G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.778-112G= MANE Select ENSP00000357980.3:n.778-112G=
ENST00000648167.1:c.460-112G= ENSP00000498033.1:n.460-112G=
ENST00000368984.7:c.778-112G= ENSP00000357980.3:n.778-112G=
NM_002775.4:c.778-112G= NP_002766.1:n.778-112G=
NM_002775.5:c.778-112G= MANE Select NP_002766.1:n.778-112G=
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