Canonical Allele Identifier: CA1181419867
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94041039A= , CM000663.2:g.94041039A= GRCh38
NC_000001.10:g.94506595A= , CM000663.1:g.94506595A= GRCh37
NC_000001.9:g.94279183A= NCBI36
NG_009073.1:g.85111T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.3522+170T= MANE Select ENSP00000359245.3:n.3522+170T=
ENST00000370225.3:c.3522+170T= ENSP00000359245.3:n.3522+170T=
ENST00000536513.5:c.-64-950T= ENSP00000439707.2:n.-64-950T=
NM_000350.2:c.3522+170T= NP_000341.2:n.3522+170T=
NM_000350.3:c.3522+170T= MANE Select NP_000341.2:n.3522+170T=