Canonical Allele Identifier: CA1142132832
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94030496C= , CM000663.2:g.94030496C= GRCh38
NC_000001.10:g.94496052C= , CM000663.1:g.94496052C= GRCh37
NC_000001.9:g.94268640C= NCBI36
NG_009073.1:g.95654G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4284G= MANE Select ENSP00000359245.3:p.Thr1428=
ENST00000370225.3:c.4284G= ENSP00000359245.3:p.Thr1428=
ENST00000536513.5:c.660G= ENSP00000439707.2:p.Thr220=
NM_000350.2:c.4284G= NP_000341.2:p.Thr1428=
NM_000350.3:c.4284G= MANE Select NP_000341.2:p.Thr1428=