Canonical Allele Identifier: CA1941478257
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122509038A= , CM000672.2:g.122509038A= GRCh38
NC_000010.10:g.124268554A= , CM000672.1:g.124268554A= GRCh37
NC_000010.9:g.124258544A= NCBI36
NG_011554.1:g.52514A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1120+268A= MANE Select ENSP00000357980.3:n.1120+268A=
ENST00000648167.1:c.802+268A= ENSP00000498033.1:n.802+268A=
ENST00000368984.7:c.1120+268A= ENSP00000357980.3:n.1120+268A=
ENST00000420892.1:c.343+268A= ENSP00000412676.1:n.343+268A=
NM_002775.4:c.1120+268A= NP_002766.1:n.1120+268A=
NM_002775.5:c.1120+268A= MANE Select NP_002766.1:n.1120+268A=