Canonical Allele Identifier: CA1143442474
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93997907C= , CM000663.2:g.93997907C= GRCh38
NC_000001.10:g.94463463C= , CM000663.1:g.94463463C= GRCh37
NC_000001.9:g.94236051C= NCBI36
NG_009073.1:g.128243G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6683G= MANE Select ENSP00000359245.3:p.Ser2228=
ENST00000370225.3:c.6683G= ENSP00000359245.3:p.Ser2228=
ENST00000536513.5:c.3059G= ENSP00000439707.2:p.Ser1020=
NM_000350.2:c.6683G= NP_000341.2:p.Ser2228=
NM_000350.3:c.6683G= MANE Select NP_000341.2:p.Ser2228=