Canonical Allele Identifier: CA1181420082
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94041419A= , CM000663.2:g.94041419A= GRCh38
NC_000001.10:g.94506975A= , CM000663.1:g.94506975A= GRCh37
NC_000001.9:g.94279563A= NCBI36
NG_009073.1:g.84731T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.3329-17T= MANE Select ENSP00000359245.3:n.3329-17T=
ENST00000370225.3:c.3329-17T= ENSP00000359245.3:n.3329-17T=
ENST00000536513.5:c.-64-1330T= ENSP00000439707.2:n.-64-1330T=
NM_000350.2:c.3329-17T= NP_000341.2:n.3329-17T=
NM_000350.3:c.3329-17T= MANE Select NP_000341.2:n.3329-17T=