Canonical Allele Identifier: CA1181405773
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93996111G= , CM000663.2:g.93996111G= GRCh38
NC_000001.10:g.94461667G= , CM000663.1:g.94461667G= GRCh37
NC_000001.9:g.94234255G= NCBI36
NG_009073.1:g.130039C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6814C= MANE Select ENSP00000359245.3:p.Gln2272=
ENST00000370225.3:c.6814C= ENSP00000359245.3:p.Gln2272=
ENST00000536513.5:c.3190C= ENSP00000439707.2:p.Gln1064=
NM_000350.2:c.6814C= NP_000341.2:p.Gln2272=
NM_000350.3:c.6814C= MANE Select NP_000341.2:p.Gln2272=