Canonical Allele Identifier: CA1181419956
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94041127A= , CM000663.2:g.94041127A= GRCh38
NC_000001.10:g.94506683A= , CM000663.1:g.94506683A= GRCh37
NC_000001.9:g.94279271A= NCBI36
NG_009073.1:g.85023T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.3522+82T= MANE Select ENSP00000359245.3:n.3522+82T=
ENST00000370225.3:c.3522+82T= ENSP00000359245.3:n.3522+82T=
ENST00000536513.5:c.-64-1038T= ENSP00000439707.2:n.-64-1038T=
NM_000350.2:c.3522+82T= NP_000341.2:n.3522+82T=
NM_000350.3:c.3522+82T= MANE Select NP_000341.2:n.3522+82T=