Canonical Allele Identifier: CA1181447793
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94111462A= , CM000663.2:g.94111462A= GRCh38
NC_000001.10:g.94577018A= , CM000663.1:g.94577018A= GRCh37
NC_000001.9:g.94349606A= NCBI36
NG_009073.1:g.14688T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.278T= MANE Select ENSP00000359245.3:p.Ile93=
ENST00000649773.1:c.278T= ENSP00000496882.1:p.Ile93=
ENST00000370225.3:c.278T= ENSP00000359245.3:p.Ile93=
NM_000350.2:c.278T= NP_000341.2:p.Ile93=
NM_000350.3:c.278T= MANE Select NP_000341.2:p.Ile93=