Canonical Allele Identifier: CA1181408183
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021353G= , CM000663.2:g.94021353G= GRCh38
NC_000001.10:g.94486909G= , CM000663.1:g.94486909G= GRCh37
NC_000001.9:g.94259497G= NCBI36
NG_009073.1:g.104797C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4905C= MANE Select ENSP00000359245.3:p.His1635=
ENST00000370225.3:c.4905C= ENSP00000359245.3:p.His1635=
ENST00000460514.1:n.399C=
ENST00000470771.1:n.15C=
ENST00000536513.5:c.1281C= ENSP00000439707.2:p.His427=
NM_000350.2:c.4905C= NP_000341.2:p.His1635=
NM_000350.3:c.4905C= MANE Select NP_000341.2:p.His1635=