Canonical Allele Identifier: CA1941472722
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122496770C= , CM000672.2:g.122496770C= GRCh38
NC_000010.10:g.124256286C= , CM000672.1:g.124256286C= GRCh37
NC_000010.9:g.124246276C= NCBI36
NG_011554.1:g.40246C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.777+7144C= MANE Select ENSP00000357980.3:n.777+7144C=
ENST00000648167.1:c.459+7144C= ENSP00000498033.1:n.459+7144C=
ENST00000368984.7:c.777+7144C= ENSP00000357980.3:n.777+7144C=
NM_002775.4:c.777+7144C= NP_002766.1:n.777+7144C=
NM_002775.5:c.777+7144C= MANE Select NP_002766.1:n.777+7144C=