Canonical Allele Identifier: CA1941459282
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461681_122461687delinsCGCTGCT , CM000672.2:g.122461681_122461687delinsCGCTGCT GRCh38
NC_000010.10:g.124221197_124221203delinsCGCTGCT , CM000672.1:g.124221197_124221203delinsCGCTGCT GRCh37
NC_000010.9:g.124211187_124211193delinsCGCTGCT NCBI36
NG_011554.1:g.5157_5163delinsCGCTGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.29_35delinsCGCTGCT MANE Select ENSP00000357980.3:p.Pro10=
ENST00000648167.1:c.154+2972_154+2978delinsCGCTGCT ENSP00000498033.1:n.154+2972_154+2978delinsCGCTGCT
ENST00000368984.7:c.29_35delinsCGCTGCT ENSP00000357980.3:p.Pro10=
NM_002775.4:c.29_35delinsCGCTGCT NP_002766.1:p.Pro10=
NM_002775.5:c.29_35delinsCGCTGCT MANE Select NP_002766.1:p.Pro10=
Search 100 bp 5'
Search 100 bp 3'