Canonical Allele Identifier: CA1141407022
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021333C= , CM000663.2:g.94021333C= GRCh38
NC_000001.10:g.94486889C= , CM000663.1:g.94486889C= GRCh37
NC_000001.9:g.94259477C= NCBI36
NG_009073.1:g.104817G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4925G= MANE Select ENSP00000359245.3:p.Ser1642=
ENST00000370225.3:c.4925G= ENSP00000359245.3:p.Ser1642=
ENST00000460514.1:n.419G=
ENST00000470771.1:n.35G=
ENST00000536513.5:c.1301G= ENSP00000439707.2:p.Ser434=
NM_000350.2:c.4925G= NP_000341.2:p.Ser1642=
NM_000350.3:c.4925G= MANE Select NP_000341.2:p.Ser1642=