Canonical Allele Identifier: CA1141899550
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94041427C= , CM000663.2:g.94041427C= GRCh38
NC_000001.10:g.94506983C= , CM000663.1:g.94506983C= GRCh37
NC_000001.9:g.94279571C= NCBI36
NG_009073.1:g.84723G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.3329-25G= MANE Select ENSP00000359245.3:n.3329-25G=
ENST00000370225.3:c.3329-25G= ENSP00000359245.3:n.3329-25G=
ENST00000536513.5:c.-64-1338G= ENSP00000439707.2:n.-64-1338G=
NM_000350.2:c.3329-25G= NP_000341.2:n.3329-25G=
NM_000350.3:c.3329-25G= MANE Select NP_000341.2:n.3329-25G=