Canonical Allele Identifier: CA1143538145
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94029446T= , CM000663.2:g.94029446T= GRCh38
NC_000001.10:g.94495002T= , CM000663.1:g.94495002T= GRCh37
NC_000001.9:g.94267590T= NCBI36
NG_009073.1:g.96704A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4538A= MANE Select ENSP00000359245.3:p.Gln1513=
ENST00000370225.3:c.4538A= ENSP00000359245.3:p.Gln1513=
ENST00000536513.5:c.914A= ENSP00000439707.2:p.Gln305=
NM_000350.2:c.4538A= NP_000341.2:p.Gln1513=
NM_000350.3:c.4538A= MANE Select NP_000341.2:p.Gln1513=