Canonical Allele Identifier: CA418812061

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94512585C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94047029C>T , CM000663.2:g.94047029C>T	GRCh38
NC_000001.10:g.94512585C>T , CM000663.1:g.94512585C>T	GRCh37
NC_000001.9:g.94285173C>T	NCBI36
NG_009073.1:g.79121G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.2808G>A MANE Select	ENSP00000359245.3:p.Lys936=
ENST00000649773.1:c.2586G>A	ENSP00000496882.1:p.Lys862=
ENST00000370225.3:c.2808G>A	ENSP00000359245.3:p.Lys936=
ENST00000536513.5:c.-64-6940G>A	ENSP00000439707.2:n.-64-6940G>A
NM_000350.2:c.2808G>A	NP_000341.2:p.Lys936=
NM_000350.3:c.2808G>A MANE Select	NP_000341.2:p.Lys936=