Canonical Allele Identifier: CA660865191
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1443891760

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461238del , CM000672.2:g.122461238del GRCh38
NC_000010.10:g.124220754del , CM000672.1:g.124220754del GRCh37
NC_000010.9:g.124210744del NCBI36
NG_011554.1:g.4714del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648167.1:c.154+2529del ENSP00000498033.1:n.154+2529del
XR_946382.1:n.123del
XR_946383.1:n.123del
XR_946384.1:n.123del
XR_946385.1:n.123del
XR_946382.2:n.151del
XR_946383.2:n.151del
XR_946384.2:n.127del
XR_946385.2:n.151del