Canonical Allele Identifier: CA341283612

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94487222G>T (hg19) ; chr1:g.94021666G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94021666G>T , CM000663.2:g.94021666G>T	GRCh38
NC_000001.10:g.94487222G>T , CM000663.1:g.94487222G>T	GRCh37
NC_000001.9:g.94259810G>T	NCBI36
NG_009073.1:g.104484C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.4822C>A MANE Select	ENSP00000359245.3:p.His1608Asn
ENST00000370225.3:c.4822C>A	ENSP00000359245.3:p.His1608Asn
ENST00000460514.1:n.316C>A
ENST00000536513.5:c.1198C>A	ENSP00000439707.2:p.His400Asn
NM_000350.2:c.4822C>A	NP_000341.2:p.His1608Asn
NM_000350.3:c.4822C>A MANE Select	NP_000341.2:p.His1608Asn