Canonical Allele Identifier: CA1941459092
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461567C= , CM000672.2:g.122461567C= GRCh38
NC_000010.10:g.124221083C= , CM000672.1:g.124221083C= GRCh37
NC_000010.9:g.124211073C= NCBI36
NG_011554.1:g.5043C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-86C= MANE Select ENSP00000357980.3:n.-86C=
ENST00000648167.1:c.154+2858C= ENSP00000498033.1:n.154+2858C=
ENST00000368984.7:c.-86C= ENSP00000357980.3:n.-86C=
NM_002775.4:c.-86C= NP_002766.1:n.-86C=
NM_002775.5:c.-86C= MANE Select NP_002766.1:n.-86C=