Canonical Allele Identifier: CA1181420009
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94041213C= , CM000663.2:g.94041213C= GRCh38
NC_000001.10:g.94506769C= , CM000663.1:g.94506769C= GRCh37
NC_000001.9:g.94279357C= NCBI36
NG_009073.1:g.84937G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.3518G= MANE Select ENSP00000359245.3:p.Ser1173=
ENST00000370225.3:c.3518G= ENSP00000359245.3:p.Ser1173=
ENST00000536513.5:c.-64-1124G= ENSP00000439707.2:n.-64-1124G=
NM_000350.2:c.3518G= NP_000341.2:p.Ser1173=
NM_000350.3:c.3518G= MANE Select NP_000341.2:p.Ser1173=