Canonical Allele Identifier: CA1142205378
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94007647C= , CM000663.2:g.94007647C= GRCh38
NC_000001.10:g.94473203C= , CM000663.1:g.94473203C= GRCh37
NC_000001.9:g.94245791C= NCBI36
NG_009073.1:g.118503G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5992G= MANE Select ENSP00000359245.3:p.Val1998=
ENST00000370225.3:c.5992G= ENSP00000359245.3:p.Val1998=
ENST00000465352.1:n.408G=
ENST00000484388.1:n.106G=
ENST00000536513.5:c.2368G= ENSP00000439707.2:p.Val790=
NM_000350.2:c.5992G= NP_000341.2:p.Val1998=
NM_000350.3:c.5992G= MANE Select NP_000341.2:p.Val1998=