Canonical Allele Identifier: CA10245913

Gene: GRAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.39970925G>A , CM000684.2:g.39970925G>A	GRCh38
NC_000022.10:g.40366929G>A , CM000684.1:g.40366929G>A	GRCh37
NC_000022.9:g.38696875G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344138.9:c.834G>A MANE Select	ENSP00000339186.4:p.Ala278=
ENST00000344138.8:c.834G>A	ENSP00000339186.4:p.Ala278=
ENST00000407075.3:c.834G>A	ENSP00000385607.3:p.Ala278=
ENST00000460449.1:n.180G>A
NM_001291824.1:c.834G>A	NP_001278753.1:p.Ala278=
NM_001291825.1:c.834G>A	NP_001278754.1:p.Ala278=
NM_001291826.1:c.618G>A	NP_001278755.1:p.Ala206=
NM_001291828.1:c.495G>A	NP_001278757.1:p.Ala165=
NM_004810.3:c.834G>A	NP_004801.1:p.Ala278=
XM_006724376.2:c.618G>A	XP_006724439.1:p.Ala206=
XM_011530515.1:c.834G>A	XP_011528817.1:p.Ala278=
XM_011530516.1:c.834G>A	XP_011528818.1:p.Ala278=
XM_006724376.3:c.618G>A	XP_006724439.1:p.Ala206=
NM_001291824.2:c.834G>A	NP_001278753.1:p.Ala278=
NM_001291826.2:c.618G>A	NP_001278755.1:p.Ala206=
NM_001291828.2:c.495G>A	NP_001278757.1:p.Ala165=
NM_004810.4:c.834G>A MANE Select	NP_004801.1:p.Ala278=