Canonical Allele Identifier: CA1941478130
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508770G= , CM000672.2:g.122508770G= GRCh38
NC_000010.10:g.124268286G= , CM000672.1:g.124268286G= GRCh37
NC_000010.9:g.124258276G= NCBI36
NG_011554.1:g.52246G=

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.1120G= MANE Select ENSP00000357980.3:p.Gly374=
ENST00000648167.1:c.802G= ENSP00000498033.1:p.Gly268=
ENST00000368984.7:c.1120G= ENSP00000357980.3:p.Gly374=
ENST00000420892.1:c.343G= ENSP00000412676.1:p.Gly115=
NM_002775.4:c.1120G= NP_002766.1:p.Gly374=
NM_002775.5:c.1120G= MANE Select NP_002766.1:p.Gly374=