Canonical Allele Identifier: CA418821792

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94487205G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94021649G>A , CM000663.2:g.94021649G>A	GRCh38
NC_000001.10:g.94487205G>A , CM000663.1:g.94487205G>A	GRCh37
NC_000001.9:g.94259793G>A	NCBI36
NG_009073.1:g.104501C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.4839C>T MANE Select	ENSP00000359245.3:p.Asp1613=
ENST00000370225.3:c.4839C>T	ENSP00000359245.3:p.Asp1613=
ENST00000460514.1:n.333C>T
ENST00000536513.5:c.1215C>T	ENSP00000439707.2:p.Asp405=
NM_000350.2:c.4839C>T	NP_000341.2:p.Asp1613=
NM_000350.3:c.4839C>T MANE Select	NP_000341.2:p.Asp1613=