Canonical Allele Identifier: CA1181426469
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94056643G= , CM000663.2:g.94056643G= GRCh38
NC_000001.10:g.94522199G= , CM000663.1:g.94522199G= GRCh37
NC_000001.9:g.94294787G= NCBI36
NG_009073.1:g.69507C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.2340C= MANE Select ENSP00000359245.3:p.Phe780=
ENST00000649773.1:c.2161-1328C= ENSP00000496882.1:n.2161-1328C=
ENST00000370225.3:c.2340C= ENSP00000359245.3:p.Phe780=
ENST00000536513.5:c.-65+6531C= ENSP00000439707.2:n.-65+6531C=
NM_000350.2:c.2340C= NP_000341.2:p.Phe780=
NM_000350.3:c.2340C= MANE Select NP_000341.2:p.Phe780=