Canonical Allele Identifier: CA418810757

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94466569G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94001013G>T , CM000663.2:g.94001013G>T	GRCh38
NC_000001.10:g.94466569G>T , CM000663.1:g.94466569G>T	GRCh37
NC_000001.9:g.94239157G>T	NCBI36
NG_009073.1:g.125137C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.6375C>A MANE Select	ENSP00000359245.3:p.Leu2125=
ENST00000370225.3:c.6375C>A	ENSP00000359245.3:p.Leu2125=
ENST00000536513.5:c.2751C>A	ENSP00000439707.2:p.Leu917=
NM_000350.2:c.6375C>A	NP_000341.2:p.Leu2125=
NM_000350.3:c.6375C>A MANE Select	NP_000341.2:p.Leu2125=