Canonical Allele Identifier: CA1941477341
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122507058C= , CM000672.2:g.122507058C= GRCh38
NC_000010.10:g.124266574C= , CM000672.1:g.124266574C= GRCh37
NC_000010.9:g.124256564C= NCBI36
NG_011554.1:g.50534C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+173C= MANE Select ENSP00000357980.3:n.972+173C=
ENST00000648167.1:c.654+173C= ENSP00000498033.1:n.654+173C=
ENST00000368984.7:c.972+173C= ENSP00000357980.3:n.972+173C=
ENST00000420892.1:c.195+173C= ENSP00000412676.1:n.195+173C=
NM_002775.4:c.972+173C= NP_002766.1:n.972+173C=
NM_002775.5:c.972+173C= MANE Select NP_002766.1:n.972+173C=