Canonical Allele Identifier: CA1181408192
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021358C= , CM000663.2:g.94021358C= GRCh38
NC_000001.10:g.94486914C= , CM000663.1:g.94486914C= GRCh37
NC_000001.9:g.94259502C= NCBI36
NG_009073.1:g.104792G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4900G= MANE Select ENSP00000359245.3:p.Ala1634=
ENST00000370225.3:c.4900G= ENSP00000359245.3:p.Ala1634=
ENST00000460514.1:n.394G=
ENST00000470771.1:n.10G=
ENST00000536513.5:c.1276G= ENSP00000439707.2:p.Ala426=
NM_000350.2:c.4900G= NP_000341.2:p.Ala1634=
NM_000350.3:c.4900G= MANE Select NP_000341.2:p.Ala1634=