Canonical Allele Identifier: CA341281552
Gene: ABCA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94015742T>A , CM000663.2:g.94015742T>A GRCh38
NC_000001.10:g.94481298T>A , CM000663.1:g.94481298T>A GRCh37
NC_000001.9:g.94253886T>A NCBI36
NG_009073.1:g.110408A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5309A>T MANE Select ENSP00000359245.3:p.Tyr1770Phe
ENST00000370225.3:c.5309A>T ENSP00000359245.3:p.Tyr1770Phe
ENST00000536513.5:c.1685A>T ENSP00000439707.2:p.Tyr562Phe
NM_000350.2:c.5309A>T NP_000341.2:p.Tyr1770Phe
NM_000350.3:c.5309A>T MANE Select NP_000341.2:p.Tyr1770Phe