Canonical Allele Identifier: CA418810727

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94466563G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94001007G>A , CM000663.2:g.94001007G>A	GRCh38
NC_000001.10:g.94466563G>A , CM000663.1:g.94466563G>A	GRCh37
NC_000001.9:g.94239151G>A	NCBI36
NG_009073.1:g.125143C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.6381C>T MANE Select	ENSP00000359245.3:p.Ser2127=
ENST00000370225.3:c.6381C>T	ENSP00000359245.3:p.Ser2127=
ENST00000536513.5:c.2757C>T	ENSP00000439707.2:p.Ser919=
NM_000350.2:c.6381C>T	NP_000341.2:p.Ser2127=
NM_000350.3:c.6381C>T MANE Select	NP_000341.2:p.Ser2127=