Canonical Allele Identifier: CA1941478249
Gene: HTRA1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122509009G= , CM000672.2:g.122509009G= GRCh38
NC_000010.10:g.124268525G= , CM000672.1:g.124268525G= GRCh37
NC_000010.9:g.124258515G= NCBI36
NG_011554.1:g.52485G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1120+239G= MANE Select ENSP00000357980.3:n.1120+239G=
ENST00000648167.1:c.802+239G= ENSP00000498033.1:n.802+239G=
ENST00000368984.7:c.1120+239G= ENSP00000357980.3:n.1120+239G=
ENST00000420892.1:c.343+239G= ENSP00000412676.1:n.343+239G=
NM_002775.4:c.1120+239G= NP_002766.1:n.1120+239G=
NM_002775.5:c.1120+239G= MANE Select NP_002766.1:n.1120+239G=
Search 100 bp 5'
Search 100 bp 3'