Canonical Allele Identifier: CA599651341

Gene: RASGRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64739155_64739156dup , CM000673.2:g.64739155_64739156dup	GRCh38
NC_000011.9:g.64506627_64506628dup , CM000673.1:g.64506627_64506628dup	GRCh37
NC_000011.8:g.64263203_64263204dup	NCBI36
NG_007574.1:g.11315_11316dup , LRG_100:g.11315_11316dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394432.8:c.813+218_813+219dup MANE Select	ENSP00000377953.3:n.813+218_813+219dup
ENST00000354024.7:c.813+218_813+219dup	ENSP00000338864.3:n.813+218_813+219dup
ENST00000377494.5:c.813+218_813+219dup	ENSP00000366714.1:n.813+218_813+219dup
ENST00000377497.7:c.813+218_813+219dup	ENSP00000366717.3:n.813+218_813+219dup
ENST00000394432.7:c.813+218_813+219dup	ENSP00000377953.3:n.813+218_813+219dup
ENST00000421556.5:c.*541+218_*541+219dup	ENSP00000401510.1:n.*541+218_*541+219dup
ENST00000464324.5:n.1162+218_1162+219dup
NM_001098670.1:c.813+218_813+219dup	NP_001092140.1:n.813+218_813+219dup
NM_001098671.1:c.813+218_813+219dup	NP_001092141.1:n.813+218_813+219dup
NM_153819.1:c.813+218_813+219dup , LRG_100t1:c.813+218_813+219dup	NP_722541.1:n.813+218_813+219dup
XM_005273707.3:c.1128+218_1128+219dup	XP_005273764.3:n.1128+218_1128+219dup
XM_011544718.1:c.1128+218_1128+219dup	XP_011543020.1:n.1128+218_1128+219dup
XM_011544719.1:c.1128+218_1128+219dup	XP_011543021.1:n.1128+218_1128+219dup
XM_011544720.1:c.813+218_813+219dup	XP_011543022.1:n.813+218_813+219dup
XM_011544721.1:c.813+218_813+219dup	XP_011543023.1:n.813+218_813+219dup
XM_011544722.1:c.813+218_813+219dup	XP_011543024.1:n.813+218_813+219dup
XM_011544723.1:c.813+218_813+219dup	XP_011543025.1:n.813+218_813+219dup
XM_011544724.1:c.813+218_813+219dup	XP_011543026.1:n.813+218_813+219dup
XM_011544725.1:c.378+218_378+219dup	XP_011543027.1:n.378+218_378+219dup
NM_001318398.1:c.378+218_378+219dup	NP_001305327.1:n.378+218_378+219dup
XM_005273707.4:c.1128+218_1128+219dup	XP_005273764.3:n.1128+218_1128+219dup
XM_011544718.2:c.1128+218_1128+219dup	XP_011543020.1:n.1128+218_1128+219dup
XM_011544720.2:c.813+218_813+219dup	XP_011543022.1:n.813+218_813+219dup
XM_011544722.2:c.813+218_813+219dup	XP_011543024.1:n.813+218_813+219dup
XM_011544723.3:c.813+218_813+219dup	XP_011543025.1:n.813+218_813+219dup
XM_011544725.2:c.378+218_378+219dup	XP_011543027.1:n.378+218_378+219dup
XM_017017082.2:c.1677+218_1677+219dup	XP_016872571.1:n.1677+218_1677+219dup
XM_017017083.2:c.1677+218_1677+219dup	XP_016872572.1:n.1677+218_1677+219dup
XM_017017084.2:c.813+218_813+219dup	XP_016872573.1:n.813+218_813+219dup
XM_017017085.2:c.636+218_636+219dup	XP_016872574.1:n.636+218_636+219dup
XM_017017086.1:c.378+218_378+219dup	XP_016872575.1:n.378+218_378+219dup
NM_001098671.2:c.813+218_813+219dup MANE Select	NP_001092141.1:n.813+218_813+219dup
NM_001098670.2:c.813+218_813+219dup	NP_001092140.1:n.813+218_813+219dup
NM_001318398.2:c.378+218_378+219dup	NP_001305327.1:n.378+218_378+219dup