Canonical Allele Identifier: CA1181422681
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94047142T= , CM000663.2:g.94047142T= GRCh38
NC_000001.10:g.94512698T= , CM000663.1:g.94512698T= GRCh37
NC_000001.9:g.94285286T= NCBI36
NG_009073.1:g.79008A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2744-49A= MANE Select ENSP00000359245.3:n.2744-49A=
ENST00000649773.1:c.2522-49A= ENSP00000496882.1:n.2522-49A=
ENST00000370225.3:c.2744-49A= ENSP00000359245.3:n.2744-49A=
ENST00000536513.5:c.-64-7053A= ENSP00000439707.2:n.-64-7053A=
NM_000350.2:c.2744-49A= NP_000341.2:n.2744-49A=
NM_000350.3:c.2744-49A= MANE Select NP_000341.2:n.2744-49A=