Canonical Allele Identifier: CA2611238755
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122461587-T-TCTCCCCGGCGCCG
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461591_122461603dup , CM000672.2:g.122461591_122461603dup GRCh38
NC_000010.10:g.124221107_124221119dup , CM000672.1:g.124221107_124221119dup GRCh37
NC_000010.9:g.124211097_124211109dup NCBI36
NG_011554.1:g.5067_5079dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-62_-50dup MANE Select ENSP00000357980.3:n.-62_-50dup
ENST00000648167.1:c.154+2882_154+2894dup ENSP00000498033.1:n.154+2882_154+2894dup
ENST00000368984.7:c.-62_-50dup ENSP00000357980.3:n.-62_-50dup
NM_002775.4:c.-62_-50dup NP_002766.1:n.-62_-50dup
NM_002775.5:c.-62_-50dup MANE Select NP_002766.1:n.-62_-50dup
Search 100 bp 5'
Search 100 bp 3'