Canonical Allele Identifier: CA1941478126
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508759G= , CM000672.2:g.122508759G= GRCh38
NC_000010.10:g.124268275G= , CM000672.1:g.124268275G= GRCh37
NC_000010.9:g.124258265G= NCBI36
NG_011554.1:g.52235G=

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.1109G= MANE Select ENSP00000357980.3:p.Arg370=
ENST00000648167.1:c.791G= ENSP00000498033.1:p.Arg264=
ENST00000368984.7:c.1109G= ENSP00000357980.3:p.Arg370=
ENST00000420892.1:c.332G= ENSP00000412676.1:p.Arg111=
NM_002775.4:c.1109G= NP_002766.1:p.Arg370=
NM_002775.5:c.1109G= MANE Select NP_002766.1:p.Arg370=