Canonical Allele Identifier: CA1941477280
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506932_122506933delinsCA , CM000672.2:g.122506932_122506933delinsCA GRCh38
NC_000010.10:g.124266448_124266449delinsCA , CM000672.1:g.124266448_124266449delinsCA GRCh37
NC_000010.9:g.124256438_124256439delinsCA NCBI36
NG_011554.1:g.50408_50409delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+47_972+48delinsCA MANE Select ENSP00000357980.3:n.972+47_972+48delinsCA
ENST00000648167.1:c.654+47_654+48delinsCA ENSP00000498033.1:n.654+47_654+48delinsCA
ENST00000368984.7:c.972+47_972+48delinsCA ENSP00000357980.3:n.972+47_972+48delinsCA
ENST00000420892.1:c.195+47_195+48delinsCA ENSP00000412676.1:n.195+47_195+48delinsCA
NM_002775.4:c.972+47_972+48delinsCA NP_002766.1:n.972+47_972+48delinsCA
NM_002775.5:c.972+47_972+48delinsCA MANE Select NP_002766.1:n.972+47_972+48delinsCA