Canonical Allele Identifier: CA1181411602
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94015746G= , CM000663.2:g.94015746G= GRCh38
NC_000001.10:g.94481302G= , CM000663.1:g.94481302G= GRCh37
NC_000001.9:g.94253890G= NCBI36
NG_009073.1:g.110404C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.5305C= MANE Select ENSP00000359245.3:p.Leu1769=
ENST00000370225.3:c.5305C= ENSP00000359245.3:p.Leu1769=
ENST00000536513.5:c.1681C= ENSP00000439707.2:p.Leu561=
NM_000350.2:c.5305C= NP_000341.2:p.Leu1769=
NM_000350.3:c.5305C= MANE Select NP_000341.2:p.Leu1769=