Canonical Allele Identifier: CA418810853

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94466592T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94001036T>G , CM000663.2:g.94001036T>G	GRCh38
NC_000001.10:g.94466592T>G , CM000663.1:g.94466592T>G	GRCh37
NC_000001.9:g.94239180T>G	NCBI36
NG_009073.1:g.125114A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.6352A>C MANE Select	ENSP00000359245.3:p.Arg2118=
ENST00000370225.3:c.6352A>C	ENSP00000359245.3:p.Arg2118=
ENST00000536513.5:c.2728A>C	ENSP00000439707.2:p.Arg910=
NM_000350.2:c.6352A>C	NP_000341.2:p.Arg2118=
NM_000350.3:c.6352A>C MANE Select	NP_000341.2:p.Arg2118=