Canonical Allele Identifier: CA957585
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2798936
ClinVar RCV Id: RCV003668231
dbSNP Id: rs763880438
gnomAD v2: 1-94495007-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94029451G>A , CM000663.2:g.94029451G>A GRCh38
NC_000001.10:g.94495007G>A , CM000663.1:g.94495007G>A GRCh37
NC_000001.9:g.94267595G>A NCBI36
NG_009073.1:g.96699C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4533C>T MANE Select ENSP00000359245.3:p.Pro1511=
ENST00000370225.3:c.4533C>T ENSP00000359245.3:p.Pro1511=
ENST00000536513.5:c.909C>T ENSP00000439707.2:p.Pro303=
NM_000350.2:c.4533C>T NP_000341.2:p.Pro1511=
NM_000350.3:c.4533C>T MANE Select NP_000341.2:p.Pro1511=