Canonical Allele Identifier: CA1181408843
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021846C= , CM000663.2:g.94021846C= GRCh38
NC_000001.10:g.94487402C= , CM000663.1:g.94487402C= GRCh37
NC_000001.9:g.94259990C= NCBI36
NG_009073.1:g.104304G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.4773G= MANE Select ENSP00000359245.3:p.Gly1591=
ENST00000370225.3:c.4773G= ENSP00000359245.3:p.Gly1591=
ENST00000460514.1:n.267G=
ENST00000536513.5:c.1149G= ENSP00000439707.2:p.Gly383=
NM_000350.2:c.4773G= NP_000341.2:p.Gly1591=
NM_000350.3:c.4773G= MANE Select NP_000341.2:p.Gly1591=