Canonical Allele Identifier: CA1941459207
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461637C= , CM000672.2:g.122461637C= GRCh38
NC_000010.10:g.124221153C= , CM000672.1:g.124221153C= GRCh37
NC_000010.9:g.124211143C= NCBI36
NG_011554.1:g.5113C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-16C= MANE Select ENSP00000357980.3:n.-16C=
ENST00000648167.1:c.154+2928C= ENSP00000498033.1:n.154+2928C=
ENST00000368984.7:c.-16C= ENSP00000357980.3:n.-16C=
NM_002775.4:c.-16C= NP_002766.1:n.-16C=
NM_002775.5:c.-16C= MANE Select NP_002766.1:n.-16C=