Canonical Allele Identifier: CA418825209

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94497358G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94031802G>C , CM000663.2:g.94031802G>C	GRCh38
NC_000001.10:g.94497358G>C , CM000663.1:g.94497358G>C	GRCh37
NC_000001.9:g.94269946G>C	NCBI36
NG_009073.1:g.94348C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.4104C>G MANE Select	ENSP00000359245.3:p.Arg1368=
ENST00000370225.3:c.4104C>G	ENSP00000359245.3:p.Arg1368=
ENST00000536513.5:c.480C>G	ENSP00000439707.2:p.Arg160=
NM_000350.2:c.4104C>G	NP_000341.2:p.Arg1368=
NM_000350.3:c.4104C>G MANE Select	NP_000341.2:p.Arg1368=