Canonical Allele Identifier: CA418812199

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94467492A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94001936A>G , CM000663.2:g.94001936A>G	GRCh38
NC_000001.10:g.94467492A>G , CM000663.1:g.94467492A>G	GRCh37
NC_000001.9:g.94240080A>G	NCBI36
NG_009073.1:g.124214T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.6204T>C MANE Select	ENSP00000359245.3:p.Ala2068=
ENST00000370225.3:c.6204T>C	ENSP00000359245.3:p.Ala2068=
ENST00000465352.1:n.620T>C
ENST00000536513.5:c.2580T>C	ENSP00000439707.2:p.Ala860=
NM_000350.2:c.6204T>C	NP_000341.2:p.Ala2068=
NM_000350.3:c.6204T>C MANE Select	NP_000341.2:p.Ala2068=