Canonical Allele Identifier: CA1181422497
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94046681T= , CM000663.2:g.94046681T= GRCh38
NC_000001.10:g.94512237T= , CM000663.1:g.94512237T= GRCh37
NC_000001.9:g.94284825T= NCBI36
NG_009073.1:g.79469A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2918+238A= MANE Select ENSP00000359245.3:n.2918+238A=
ENST00000649773.1:c.2696+238A= ENSP00000496882.1:n.2696+238A=
ENST00000370225.3:c.2918+238A= ENSP00000359245.3:n.2918+238A=
ENST00000536513.5:c.-64-6592A= ENSP00000439707.2:n.-64-6592A=
NM_000350.2:c.2918+238A= NP_000341.2:n.2918+238A=
NM_000350.3:c.2918+238A= MANE Select NP_000341.2:n.2918+238A=