Canonical Allele Identifier: CA418812152

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94512600C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94047044C>A , CM000663.2:g.94047044C>A	GRCh38
NC_000001.10:g.94512600C>A , CM000663.1:g.94512600C>A	GRCh37
NC_000001.9:g.94285188C>A	NCBI36
NG_009073.1:g.79106G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.2793G>T MANE Select	ENSP00000359245.3:p.Val931=
ENST00000649773.1:c.2571G>T	ENSP00000496882.1:p.Val857=
ENST00000370225.3:c.2793G>T	ENSP00000359245.3:p.Val931=
ENST00000536513.5:c.-64-6955G>T	ENSP00000439707.2:n.-64-6955G>T
NM_000350.2:c.2793G>T	NP_000341.2:p.Val931=
NM_000350.3:c.2793G>T MANE Select	NP_000341.2:p.Val931=