Canonical Allele Identifier: CA1941467453
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472221C= , CM000672.2:g.122472221C= GRCh38
NC_000010.10:g.124231737C= , CM000672.1:g.124231737C= GRCh37
NC_000010.9:g.124221727C= NCBI36
NG_011554.1:g.15697C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10097C= MANE Select ENSP00000357980.3:n.472+10097C=
ENST00000648167.1:c.154+13512C= ENSP00000498033.1:n.154+13512C=
ENST00000368984.7:c.472+10097C= ENSP00000357980.3:n.472+10097C=
NM_002775.4:c.472+10097C= NP_002766.1:n.472+10097C=
NM_002775.5:c.472+10097C= MANE Select NP_002766.1:n.472+10097C=