Canonical Allele Identifier: CA5726044
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs746189509

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.1109G>C MANE Select ENSP00000357980.3:p.Arg370Pro
ENST00000648167.1:c.791G>C ENSP00000498033.1:p.Arg264Pro
ENST00000368984.7:c.1109G>C ENSP00000357980.3:p.Arg370Pro
ENST00000420892.1:c.332G>C ENSP00000412676.1:p.Arg111Pro
NM_002775.4:c.1109G>C NP_002766.1:p.Arg370Pro
NM_002775.5:c.1109G>C MANE Select NP_002766.1:p.Arg370Pro