Canonical Allele Identifier: CA1181414561
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94029484T= , CM000663.2:g.94029484T= GRCh38
NC_000001.10:g.94495040T= , CM000663.1:g.94495040T= GRCh37
NC_000001.9:g.94267628T= NCBI36
NG_009073.1:g.96666A=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.4500A= MANE Select ENSP00000359245.3:p.Pro1500=
ENST00000370225.3:c.4500A= ENSP00000359245.3:p.Pro1500=
ENST00000536513.5:c.876A= ENSP00000439707.2:p.Pro292=
NM_000350.2:c.4500A= NP_000341.2:p.Pro1500=
NM_000350.3:c.4500A= MANE Select NP_000341.2:p.Pro1500=