Canonical Allele Identifier: CA341287117
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2035923
ClinVar RCV Id: RCV002894573
MyVariant Identifiers: chr1:g.94497422C>T (hg19) chr1:g.94031866C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94031866C>T , CM000663.2:g.94031866C>T GRCh38
NC_000001.10:g.94497422C>T , CM000663.1:g.94497422C>T GRCh37
NC_000001.9:g.94270010C>T NCBI36
NG_009073.1:g.94284G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4040G>A MANE Select ENSP00000359245.3:p.Gly1347Glu
ENST00000370225.3:c.4040G>A ENSP00000359245.3:p.Gly1347Glu
ENST00000536513.5:c.416G>A ENSP00000439707.2:p.Gly139Glu
NM_000350.2:c.4040G>A NP_000341.2:p.Gly1347Glu
NM_000350.3:c.4040G>A MANE Select NP_000341.2:p.Gly1347Glu
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