Canonical Allele Identifier: CA341283669

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94487249A>G (hg19) ; chr1:g.94021693A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94021693A>G , CM000663.2:g.94021693A>G	GRCh38
NC_000001.10:g.94487249A>G , CM000663.1:g.94487249A>G	GRCh37
NC_000001.9:g.94259837A>G	NCBI36
NG_009073.1:g.104457T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.4795T>C MANE Select	ENSP00000359245.3:p.Ser1599Pro
ENST00000370225.3:c.4795T>C	ENSP00000359245.3:p.Ser1599Pro
ENST00000460514.1:n.289T>C
ENST00000536513.5:c.1171T>C	ENSP00000439707.2:p.Ser391Pro
NM_000350.2:c.4795T>C	NP_000341.2:p.Ser1599Pro
NM_000350.3:c.4795T>C MANE Select	NP_000341.2:p.Ser1599Pro