Canonical Allele Identifier: CA1941477068
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506448_122506450delinsGGT , CM000672.2:g.122506448_122506450delinsGGT GRCh38
NC_000010.10:g.124265964_124265966delinsGGT , CM000672.1:g.124265964_124265966delinsGGT GRCh37
NC_000010.9:g.124255954_124255956delinsGGT NCBI36
NG_011554.1:g.49924_49926delinsGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.778-243_778-241delinsGGT MANE Select ENSP00000357980.3:n.778-243_778-241delinsGGT
ENST00000648167.1:c.460-243_460-241delinsGGT ENSP00000498033.1:n.460-243_460-241delinsGGT
ENST00000368984.7:c.778-243_778-241delinsGGT ENSP00000357980.3:n.778-243_778-241delinsGGT
NM_002775.4:c.778-243_778-241delinsGGT NP_002766.1:n.778-243_778-241delinsGGT
NM_002775.5:c.778-243_778-241delinsGGT MANE Select NP_002766.1:n.778-243_778-241delinsGGT