Canonical Allele Identifier: CA1941467407
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472126C= , CM000672.2:g.122472126C= GRCh38
NC_000010.10:g.124231642C= , CM000672.1:g.124231642C= GRCh37
NC_000010.9:g.124221632C= NCBI36
NG_011554.1:g.15602C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10002C= MANE Select ENSP00000357980.3:n.472+10002C=
ENST00000648167.1:c.154+13417C= ENSP00000498033.1:n.154+13417C=
ENST00000368984.7:c.472+10002C= ENSP00000357980.3:n.472+10002C=
NM_002775.4:c.472+10002C= NP_002766.1:n.472+10002C=
NM_002775.5:c.472+10002C= MANE Select NP_002766.1:n.472+10002C=