Canonical Allele Identifier: CA1941478029
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508490G= , CM000672.2:g.122508490G= GRCh38
NC_000010.10:g.124268006G= , CM000672.1:g.124268006G= GRCh37
NC_000010.9:g.124257996G= NCBI36
NG_011554.1:g.51966G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1006-166G= MANE Select ENSP00000357980.3:n.1006-166G=
ENST00000648167.1:c.688-166G= ENSP00000498033.1:n.688-166G=
ENST00000368984.7:c.1006-166G= ENSP00000357980.3:n.1006-166G=
ENST00000420892.1:c.229-166G= ENSP00000412676.1:n.229-166G=
NM_002775.4:c.1006-166G= NP_002766.1:n.1006-166G=
NM_002775.5:c.1006-166G= MANE Select NP_002766.1:n.1006-166G=
Search 100 bp 5'
Search 100 bp 3'