Canonical Allele Identifier: CA1941467532
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472358_122472371delinsTTTCTTTATTACTA , CM000672.2:g.122472358_122472371delinsTTTCTTTATTACTA GRCh38
NC_000010.10:g.124231874_124231887delinsTTTCTTTATTACTA , CM000672.1:g.124231874_124231887delinsTTTCTTTATTACTA GRCh37
NC_000010.9:g.124221864_124221877delinsTTTCTTTATTACTA NCBI36
NG_011554.1:g.15834_15847delinsTTTCTTTATTACTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10234_472+10247delinsTTTCTTTATTACTA MANE Select ENSP00000357980.3:n.472+10234_472+10247delinsTTTCTTTATTACTA
ENST00000648167.1:c.154+13649_154+13662delinsTTTCTTTATTACTA ENSP00000498033.1:n.154+13649_154+13662delinsTTTCTTTATTACTA
ENST00000368984.7:c.472+10234_472+10247delinsTTTCTTTATTACTA ENSP00000357980.3:n.472+10234_472+10247delinsTTTCTTTATTACTA
NM_002775.4:c.472+10234_472+10247delinsTTTCTTTATTACTA NP_002766.1:n.472+10234_472+10247delinsTTTCTTTATTACTA
NM_002775.5:c.472+10234_472+10247delinsTTTCTTTATTACTA MANE Select NP_002766.1:n.472+10234_472+10247delinsTTTCTTTATTACTA