Canonical Allele Identifier: CA1143640824
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94015725C= , CM000663.2:g.94015725C= GRCh38
NC_000001.10:g.94481281C= , CM000663.1:g.94481281C= GRCh37
NC_000001.9:g.94253869C= NCBI36
NG_009073.1:g.110425G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5312+14G= MANE Select ENSP00000359245.3:n.5312+14G=
ENST00000370225.3:c.5312+14G= ENSP00000359245.3:n.5312+14G=
ENST00000536513.5:c.1688+14G= ENSP00000439707.2:n.1688+14G=
NM_000350.2:c.5312+14G= NP_000341.2:n.5312+14G=
NM_000350.3:c.5312+14G= MANE Select NP_000341.2:n.5312+14G=