Canonical Allele Identifier: CA1181422635
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94047051A= , CM000663.2:g.94047051A= GRCh38
NC_000001.10:g.94512607A= , CM000663.1:g.94512607A= GRCh37
NC_000001.9:g.94285195A= NCBI36
NG_009073.1:g.79099T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2786T= MANE Select ENSP00000359245.3:p.Val929=
ENST00000649773.1:c.2564T= ENSP00000496882.1:p.Val855=
ENST00000370225.3:c.2786T= ENSP00000359245.3:p.Val929=
ENST00000536513.5:c.-64-6962T= ENSP00000439707.2:n.-64-6962T=
NM_000350.2:c.2786T= NP_000341.2:p.Val929=
NM_000350.3:c.2786T= MANE Select NP_000341.2:p.Val929=