Canonical Allele Identifier: CA1181408200
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021359C= , CM000663.2:g.94021359C= GRCh38
NC_000001.10:g.94486915C= , CM000663.1:g.94486915C= GRCh37
NC_000001.9:g.94259503C= NCBI36
NG_009073.1:g.104791G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4899G= MANE Select ENSP00000359245.3:p.Val1633=
ENST00000370225.3:c.4899G= ENSP00000359245.3:p.Val1633=
ENST00000460514.1:n.393G=
ENST00000470771.1:n.9G=
ENST00000536513.5:c.1275G= ENSP00000439707.2:p.Val425=
NM_000350.2:c.4899G= NP_000341.2:p.Val1633=
NM_000350.3:c.4899G= MANE Select NP_000341.2:p.Val1633=