Canonical Allele Identifier: CA1181414517
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94029388C= , CM000663.2:g.94029388C= GRCh38
NC_000001.10:g.94494944C= , CM000663.1:g.94494944C= GRCh37
NC_000001.9:g.94267532C= NCBI36
NG_009073.1:g.96762G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4539+57G= MANE Select ENSP00000359245.3:n.4539+57G=
ENST00000370225.3:c.4539+57G= ENSP00000359245.3:n.4539+57G=
ENST00000536513.5:c.915+57G= ENSP00000439707.2:n.915+57G=
NM_000350.2:c.4539+57G= NP_000341.2:n.4539+57G=
NM_000350.3:c.4539+57G= MANE Select NP_000341.2:n.4539+57G=