Canonical Allele Identifier: CA418819758
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94481321G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94015765G>A , CM000663.2:g.94015765G>A GRCh38
NC_000001.10:g.94481321G>A , CM000663.1:g.94481321G>A GRCh37
NC_000001.9:g.94253909G>A NCBI36
NG_009073.1:g.110385C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5286C>T MANE Select ENSP00000359245.3:p.Ala1762=
ENST00000370225.3:c.5286C>T ENSP00000359245.3:p.Ala1762=
ENST00000536513.5:c.1662C>T ENSP00000439707.2:p.Ala554=
NM_000350.2:c.5286C>T NP_000341.2:p.Ala1762=
NM_000350.3:c.5286C>T MANE Select NP_000341.2:p.Ala1762=