Canonical Allele Identifier: CA1142115957
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94015744C= , CM000663.2:g.94015744C= GRCh38
NC_000001.10:g.94481300C= , CM000663.1:g.94481300C= GRCh37
NC_000001.9:g.94253888C= NCBI36
NG_009073.1:g.110406G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.5307G= MANE Select ENSP00000359245.3:p.Leu1769=
ENST00000370225.3:c.5307G= ENSP00000359245.3:p.Leu1769=
ENST00000536513.5:c.1683G= ENSP00000439707.2:p.Leu561=
NM_000350.2:c.5307G= NP_000341.2:p.Leu1769=
NM_000350.3:c.5307G= MANE Select NP_000341.2:p.Leu1769=