Canonical Allele Identifier: CA1181422585
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94046931T= , CM000663.2:g.94046931T= GRCh38
NC_000001.10:g.94512487T= , CM000663.1:g.94512487T= GRCh37
NC_000001.9:g.94285075T= NCBI36
NG_009073.1:g.79219A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2906A= MANE Select ENSP00000359245.3:p.Lys969=
ENST00000649773.1:c.2684A= ENSP00000496882.1:p.Lys895=
ENST00000370225.3:c.2906A= ENSP00000359245.3:p.Lys969=
ENST00000536513.5:c.-64-6842A= ENSP00000439707.2:n.-64-6842A=
NM_000350.2:c.2906A= NP_000341.2:p.Lys969=
NM_000350.3:c.2906A= MANE Select NP_000341.2:p.Lys969=