Canonical Allele Identifier: CA418811606

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94512525G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94046969G>A , CM000663.2:g.94046969G>A	GRCh38
NC_000001.10:g.94512525G>A , CM000663.1:g.94512525G>A	GRCh37
NC_000001.9:g.94285113G>A	NCBI36
NG_009073.1:g.79181C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.2868C>T MANE Select	ENSP00000359245.3:p.Asn956=
ENST00000649773.1:c.2646C>T	ENSP00000496882.1:p.Asn882=
ENST00000370225.3:c.2868C>T	ENSP00000359245.3:p.Asn956=
ENST00000536513.5:c.-64-6880C>T	ENSP00000439707.2:n.-64-6880C>T
NM_000350.2:c.2868C>T	NP_000341.2:p.Asn956=
NM_000350.3:c.2868C>T MANE Select	NP_000341.2:p.Asn956=