Canonical Allele Identifier: CA341283674

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94487252C>A (hg19) ; chr1:g.94021696C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94021696C>A , CM000663.2:g.94021696C>A	GRCh38
NC_000001.10:g.94487252C>A , CM000663.1:g.94487252C>A	GRCh37
NC_000001.9:g.94259840C>A	NCBI36
NG_009073.1:g.104454G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.4792G>T MANE Select	ENSP00000359245.3:p.Ala1598Ser
ENST00000370225.3:c.4792G>T	ENSP00000359245.3:p.Ala1598Ser
ENST00000460514.1:n.286G>T
ENST00000536513.5:c.1168G>T	ENSP00000439707.2:p.Ala390Ser
NM_000350.2:c.4792G>T	NP_000341.2:p.Ala1598Ser
NM_000350.3:c.4792G>T MANE Select	NP_000341.2:p.Ala1598Ser