Canonical Allele Identifier: CA1941477062
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506438C= , CM000672.2:g.122506438C= GRCh38
NC_000010.10:g.124265954C= , CM000672.1:g.124265954C= GRCh37
NC_000010.9:g.124255944C= NCBI36
NG_011554.1:g.49914C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.778-253C= MANE Select ENSP00000357980.3:n.778-253C=
ENST00000648167.1:c.460-253C= ENSP00000498033.1:n.460-253C=
ENST00000368984.7:c.778-253C= ENSP00000357980.3:n.778-253C=
NM_002775.4:c.778-253C= NP_002766.1:n.778-253C=
NM_002775.5:c.778-253C= MANE Select NP_002766.1:n.778-253C=