Canonical Allele Identifier: CA6079355

Gene: RASGRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64741966T>C , CM000673.2:g.64741966T>C	GRCh38
NC_000011.9:g.64509438T>C , CM000673.1:g.64509438T>C	GRCh37
NC_000011.8:g.64266014T>C	NCBI36
NG_007574.1:g.8491A>G , LRG_100:g.8491A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001098671.2:c.176+44A>G MANE Select	NP_001092141.1:n.176+44A>G
ENST00000394432.8:c.176+44A>G MANE Select	ENSP00000377953.3:n.176+44A>G
NM_001098670.1:c.176+44A>G	NP_001092140.1:n.176+44A>G
NM_001098670.2:c.176+44A>G	NP_001092140.1:n.176+44A>G
NM_001098671.1:c.176+44A>G	NP_001092141.1:n.176+44A>G
NM_001318398.1:c.-260+44A>G	NP_001305327.1:n.-260+44A>G
NM_001318398.2:c.-260+44A>G	NP_001305327.1:n.-260+44A>G
NM_153819.1:c.176+44A>G , LRG_100t1:c.176+44A>G	NP_722541.1:n.176+44A>G
ENST00000354024.7:c.176+44A>G	ENSP00000338864.3:n.176+44A>G
ENST00000377485.5:c.176+44A>G	ENSP00000366705.1:n.176+44A>G
ENST00000377486.7:c.176+44A>G	ENSP00000366706.3:n.176+44A>G
ENST00000377487.5:c.176+44A>G	ENSP00000366707.1:n.176+44A>G
ENST00000377489.5:c.176+44A>G	ENSP00000366709.1:n.176+44A>G
ENST00000377494.5:c.176+44A>G	ENSP00000366714.1:n.176+44A>G
ENST00000377497.7:c.176+44A>G	ENSP00000366717.3:n.176+44A>G
ENST00000394428.5:c.96+44A>G	ENSP00000377949.1:n.96+44A>G
ENST00000394429.5:c.74-433A>G	ENSP00000377950.1:n.74-433A>G
ENST00000394430.5:c.176+44A>G	ENSP00000377951.1:n.176+44A>G
ENST00000394432.7:c.176+44A>G	ENSP00000377953.3:n.176+44A>G
ENST00000421556.5:c.96+44A>G	ENSP00000401510.1:n.96+44A>G
ENST00000430645.1:c.176+44A>G	ENSP00000401314.1:n.176+44A>G
ENST00000431822.5:c.176+44A>G	ENSP00000399114.1:n.176+44A>G
ENST00000441258.5:c.176+44A>G	ENSP00000399028.1:n.176+44A>G
ENST00000445445.5:c.176+44A>G	ENSP00000396029.1:n.176+44A>G
XM_005273707.3:c.491+44A>G	XP_005273764.3:n.491+44A>G
XM_005273707.4:c.491+44A>G	XP_005273764.3:n.491+44A>G
XM_011544718.1:c.491+44A>G	XP_011543020.1:n.491+44A>G
XM_011544718.2:c.491+44A>G	XP_011543020.1:n.491+44A>G
XM_011544719.1:c.491+44A>G	XP_011543021.1:n.491+44A>G
XM_011544720.1:c.176+44A>G	XP_011543022.1:n.176+44A>G
XM_011544720.2:c.176+44A>G	XP_011543022.1:n.176+44A>G
XM_011544721.1:c.176+44A>G	XP_011543023.1:n.176+44A>G
XM_011544722.1:c.176+44A>G	XP_011543024.1:n.176+44A>G
XM_011544722.2:c.176+44A>G	XP_011543024.1:n.176+44A>G
XM_011544723.1:c.176+44A>G	XP_011543025.1:n.176+44A>G
XM_011544723.3:c.176+44A>G	XP_011543025.1:n.176+44A>G
XM_011544724.1:c.176+44A>G	XP_011543026.1:n.176+44A>G
XM_011544725.2:c.-342+44A>G	XP_011543027.1:n.-342+44A>G
XM_017017082.2:c.1040+44A>G	XP_016872571.1:n.1040+44A>G
XM_017017083.2:c.1040+44A>G	XP_016872572.1:n.1040+44A>G
XM_017017084.2:c.176+44A>G	XP_016872573.1:n.176+44A>G
XR_001747719.2:n.1928+44A>G
XR_001747720.2:n.1928+44A>G