Canonical Allele Identifier: CA223887023

Gene: RASGRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64727529_64727530del , CM000673.2:g.64727529_64727530del	GRCh38
NC_000011.9:g.64495001_64495002del , CM000673.1:g.64495001_64495002del	GRCh37
NC_000011.8:g.64251577_64251578del	NCBI36
NG_007574.1:g.22949_22950del , LRG_100:g.22949_22950del
NG_047107.1:g.681_682del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394432.8:c.1772-148_1772-147del MANE Select	ENSP00000377953.3:n.1772-148_1772-147del
ENST00000354024.7:c.1772-148_1772-147del	ENSP00000338864.3:n.1772-148_1772-147del
ENST00000377494.5:c.1772-145_1772-144del	ENSP00000366714.1:n.1772-145_1772-144del
ENST00000377497.7:c.1772-148_1772-147del	ENSP00000366717.3:n.1772-148_1772-147del
ENST00000394432.7:c.1772-148_1772-147del	ENSP00000377953.3:n.1772-148_1772-147del
ENST00000421556.5:c.*1500-148_*1500-147del	ENSP00000401510.1:n.*1500-148_*1500-147del
ENST00000464324.5:n.2121-145_2121-144del
ENST00000488071.1:n.515-148_515-147del
NM_001098670.1:c.1772-148_1772-147del	NP_001092140.1:n.1772-148_1772-147del
NM_001098671.1:c.1772-148_1772-147del	NP_001092141.1:n.1772-148_1772-147del
NM_153819.1:c.1772-148_1772-147del , LRG_100t1:c.1772-148_1772-147del	NP_722541.1:n.1772-148_1772-147del
XM_005273707.3:c.2087-148_2087-147del	XP_005273764.3:n.2087-148_2087-147del
XM_011544718.1:c.2087-145_2087-144del	XP_011543020.1:n.2087-145_2087-144del
XM_011544719.1:c.2087-145_2087-144del	XP_011543021.1:n.2087-145_2087-144del
XM_011544720.1:c.1772-145_1772-144del	XP_011543022.1:n.1772-145_1772-144del
XM_011544721.1:c.1772-145_1772-144del	XP_011543023.1:n.1772-145_1772-144del
XM_011544722.1:c.1772-145_1772-144del	XP_011543024.1:n.1772-145_1772-144del
XM_011544723.1:c.1772-145_1772-144del	XP_011543025.1:n.1772-145_1772-144del
XM_011544724.1:c.1772-145_1772-144del	XP_011543026.1:n.1772-145_1772-144del
XM_011544725.1:c.1337-145_1337-144del	XP_011543027.1:n.1337-145_1337-144del
NM_001318398.1:c.1337-148_1337-147del	NP_001305327.1:n.1337-148_1337-147del
XM_005273707.4:c.2087-148_2087-147del	XP_005273764.3:n.2087-148_2087-147del
XM_011544718.2:c.2087-145_2087-144del	XP_011543020.1:n.2087-145_2087-144del
XM_011544720.2:c.1772-145_1772-144del	XP_011543022.1:n.1772-145_1772-144del
XM_011544722.2:c.1772-145_1772-144del	XP_011543024.1:n.1772-145_1772-144del
XM_011544723.3:c.1772-145_1772-144del	XP_011543025.1:n.1772-145_1772-144del
XM_011544725.2:c.1337-145_1337-144del	XP_011543027.1:n.1337-145_1337-144del
XM_017017082.2:c.2636-145_2636-144del	XP_016872571.1:n.2636-145_2636-144del
XM_017017083.2:c.2636-148_2636-147del	XP_016872572.1:n.2636-148_2636-147del
XM_017017084.2:c.1772-145_1772-144del	XP_016872573.1:n.1772-145_1772-144del
XM_017017085.2:c.1595-145_1595-144del	XP_016872574.1:n.1595-145_1595-144del
XM_017017086.1:c.1337-145_1337-144del	XP_016872575.1:n.1337-145_1337-144del
NM_001098671.2:c.1772-148_1772-147del MANE Select	NP_001092141.1:n.1772-148_1772-147del
NM_001098670.2:c.1772-148_1772-147del	NP_001092140.1:n.1772-148_1772-147del
NM_001318398.2:c.1337-148_1337-147del	NP_001305327.1:n.1337-148_1337-147del