Canonical Allele Identifier: CA10245790

Gene: GRAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.39968048C>T , CM000684.2:g.39968048C>T	GRCh38
NC_000022.10:g.40364052C>T , CM000684.1:g.40364052C>T	GRCh37
NC_000022.9:g.38693998C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344138.9:c.466C>T MANE Select	ENSP00000339186.4:p.Arg156Trp
ENST00000344138.8:c.466C>T	ENSP00000339186.4:p.Arg156Trp
ENST00000407075.3:c.466C>T	ENSP00000385607.3:p.Arg156Trp
ENST00000481263.1:n.116C>T
NM_001291824.1:c.466C>T	NP_001278753.1:p.Arg156Trp
NM_001291825.1:c.466C>T	NP_001278754.1:p.Arg156Trp
NM_001291826.1:c.250C>T	NP_001278755.1:p.Arg84Trp
NM_001291828.1:c.127C>T	NP_001278757.1:p.Arg43Trp
NM_004810.3:c.466C>T	NP_004801.1:p.Arg156Trp
XM_006724376.2:c.250C>T	XP_006724439.1:p.Arg84Trp
XM_011530515.1:c.466C>T	XP_011528817.1:p.Arg156Trp
XM_011530516.1:c.466C>T	XP_011528818.1:p.Arg156Trp
XM_006724376.3:c.250C>T	XP_006724439.1:p.Arg84Trp
NM_001291824.2:c.466C>T	NP_001278753.1:p.Arg156Trp
NM_001291826.2:c.250C>T	NP_001278755.1:p.Arg84Trp
NM_001291828.2:c.127C>T	NP_001278757.1:p.Arg43Trp
NM_004810.4:c.466C>T MANE Select	NP_004801.1:p.Arg156Trp