Canonical Allele Identifier: CA1181418829
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94062646T= , CM000663.2:g.94062646T= GRCh38
NC_000001.10:g.94528202T= , CM000663.1:g.94528202T= GRCh37
NC_000001.9:g.94300790T= NCBI36
NG_009073.1:g.63504A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1868A= MANE Select ENSP00000359245.3:p.Gln623=
ENST00000649773.1:c.1868A= ENSP00000496882.1:p.Gln623=
ENST00000370225.3:c.1868A= ENSP00000359245.3:p.Gln623=
ENST00000536513.5:c.-65+528A= ENSP00000439707.2:n.-65+528A=
NM_000350.2:c.1868A= NP_000341.2:p.Gln623=
NM_000350.3:c.1868A= MANE Select NP_000341.2:p.Gln623=