Canonical Allele Identifier: CA10245806

Gene: GRAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.39968118G>A , CM000684.2:g.39968118G>A	GRCh38
NC_000022.10:g.40364122G>A , CM000684.1:g.40364122G>A	GRCh37
NC_000022.9:g.38694068G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344138.9:c.536G>A MANE Select	ENSP00000339186.4:p.Arg179Gln
ENST00000344138.8:c.536G>A	ENSP00000339186.4:p.Arg179Gln
ENST00000407075.3:c.536G>A	ENSP00000385607.3:p.Arg179Gln
ENST00000481263.1:n.186G>A
NM_001291824.1:c.536G>A	NP_001278753.1:p.Arg179Gln
NM_001291825.1:c.536G>A	NP_001278754.1:p.Arg179Gln
NM_001291826.1:c.320G>A	NP_001278755.1:p.Arg107Gln
NM_001291828.1:c.197G>A	NP_001278757.1:p.Arg66Gln
NM_004810.3:c.536G>A	NP_004801.1:p.Arg179Gln
XM_006724376.2:c.320G>A	XP_006724439.1:p.Arg107Gln
XM_011530515.1:c.536G>A	XP_011528817.1:p.Arg179Gln
XM_011530516.1:c.536G>A	XP_011528818.1:p.Arg179Gln
XM_006724376.3:c.320G>A	XP_006724439.1:p.Arg107Gln
NM_001291824.2:c.536G>A	NP_001278753.1:p.Arg179Gln
NM_001291826.2:c.320G>A	NP_001278755.1:p.Arg107Gln
NM_001291828.2:c.197G>A	NP_001278757.1:p.Arg66Gln
NM_004810.4:c.536G>A MANE Select	NP_004801.1:p.Arg179Gln