Canonical Allele Identifier: CA378606389
Gene: HTRA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122462074G>C , CM000672.2:g.122462074G>C GRCh38
NC_000010.10:g.124221590G>C , CM000672.1:g.124221590G>C GRCh37
NC_000010.9:g.124211580G>C NCBI36
NG_011554.1:g.5550G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.422G>C MANE Select ENSP00000357980.3:p.Arg141Thr
ENST00000648167.1:c.154+3365G>C ENSP00000498033.1:n.154+3365G>C
ENST00000368984.7:c.422G>C ENSP00000357980.3:p.Arg141Thr
NM_002775.4:c.422G>C NP_002766.1:p.Arg141Thr
NM_002775.5:c.422G>C MANE Select NP_002766.1:p.Arg141Thr