Canonical Allele Identifier: CA341285788

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94496032A>C (hg19) ; chr1:g.94030476A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94030476A>C , CM000663.2:g.94030476A>C	GRCh38
NC_000001.10:g.94496032A>C , CM000663.1:g.94496032A>C	GRCh37
NC_000001.9:g.94268620A>C	NCBI36
NG_009073.1:g.95674T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.4304T>G MANE Select	ENSP00000359245.3:p.Leu1435Arg
ENST00000370225.3:c.4304T>G	ENSP00000359245.3:p.Leu1435Arg
ENST00000536513.5:c.680T>G	ENSP00000439707.2:p.Leu227Arg
NM_000350.2:c.4304T>G	NP_000341.2:p.Leu1435Arg
NM_000350.3:c.4304T>G MANE Select	NP_000341.2:p.Leu1435Arg