Canonical Allele Identifier: CA418808644

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94463545T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.93997989T>G , CM000663.2:g.93997989T>G	GRCh38
NC_000001.10:g.94463545T>G , CM000663.1:g.94463545T>G	GRCh37
NC_000001.9:g.94236133T>G	NCBI36
NG_009073.1:g.128161A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.6601A>C MANE Select	ENSP00000359245.3:p.Arg2201=
ENST00000370225.3:c.6601A>C	ENSP00000359245.3:p.Arg2201=
ENST00000536513.5:c.2977A>C	ENSP00000439707.2:p.Arg993=
NM_000350.2:c.6601A>C	NP_000341.2:p.Arg2201=
NM_000350.3:c.6601A>C MANE Select	NP_000341.2:p.Arg2201=