Canonical Allele Identifier: CA1181428060
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94060677T= , CM000663.2:g.94060677T= GRCh38
NC_000001.10:g.94526233T= , CM000663.1:g.94526233T= GRCh37
NC_000001.9:g.94298821T= NCBI36
NG_009073.1:g.65473A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2020A= MANE Select ENSP00000359245.3:p.Ile674=
ENST00000649773.1:c.2020A= ENSP00000496882.1:p.Ile674=
ENST00000370225.3:c.2020A= ENSP00000359245.3:p.Ile674=
ENST00000472033.1:n.140A=
ENST00000536513.5:c.-65+2497A= ENSP00000439707.2:n.-65+2497A=
NM_000350.2:c.2020A= NP_000341.2:p.Ile674=
NM_000350.3:c.2020A= MANE Select NP_000341.2:p.Ile674=