Canonical Allele Identifier: CA1140725872
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94043413G= , CM000663.2:g.94043413G= GRCh38
NC_000001.10:g.94508969G= , CM000663.1:g.94508969G= GRCh37
NC_000001.9:g.94281557G= NCBI36
NG_009073.1:g.82737C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.3113C= MANE Select ENSP00000359245.3:p.Ala1038=
ENST00000370225.3:c.3113C= ENSP00000359245.3:p.Ala1038=
ENST00000536513.5:c.-64-3324C= ENSP00000439707.2:n.-64-3324C=
NM_000350.2:c.3113C= NP_000341.2:p.Ala1038=
NM_000350.3:c.3113C= MANE Select NP_000341.2:p.Ala1038=