Canonical Allele Identifier: CA1181414505
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94029367A= , CM000663.2:g.94029367A= GRCh38
NC_000001.10:g.94494923A= , CM000663.1:g.94494923A= GRCh37
NC_000001.9:g.94267511A= NCBI36
NG_009073.1:g.96783T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4539+78T= MANE Select ENSP00000359245.3:n.4539+78T=
ENST00000370225.3:c.4539+78T= ENSP00000359245.3:n.4539+78T=
ENST00000536513.5:c.915+78T= ENSP00000439707.2:n.915+78T=
NM_000350.2:c.4539+78T= NP_000341.2:n.4539+78T=
NM_000350.3:c.4539+78T= MANE Select NP_000341.2:n.4539+78T=