Canonical Allele Identifier: CA6078999

Gene: RASGRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64735891G>A , CM000673.2:g.64735891G>A	GRCh38
NC_000011.9:g.64503363G>A , CM000673.1:g.64503363G>A	GRCh37
NC_000011.8:g.64259939G>A	NCBI36
NG_007574.1:g.14566C>T , LRG_100:g.14566C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394432.8:c.1173+12C>T MANE Select	ENSP00000377953.3:n.1173+12C>T
ENST00000354024.7:c.1173+12C>T	ENSP00000338864.3:n.1173+12C>T
ENST00000377494.5:c.1173+12C>T	ENSP00000366714.1:n.1173+12C>T
ENST00000377497.7:c.1173+12C>T	ENSP00000366717.3:n.1173+12C>T
ENST00000394432.7:c.1173+12C>T	ENSP00000377953.3:n.1173+12C>T
ENST00000421556.5:c.*901+12C>T	ENSP00000401510.1:n.*901+12C>T
ENST00000464324.5:n.1522+12C>T
ENST00000465852.1:n.570+12C>T
ENST00000494001.5:n.372C>T
ENST00000497441.5:n.580+12C>T
NM_001098670.1:c.1173+12C>T	NP_001092140.1:n.1173+12C>T
NM_001098671.1:c.1173+12C>T	NP_001092141.1:n.1173+12C>T
NM_153819.1:c.1173+12C>T , LRG_100t1:c.1173+12C>T	NP_722541.1:n.1173+12C>T
XM_005273707.3:c.1488+12C>T	XP_005273764.3:n.1488+12C>T
XM_011544718.1:c.1488+12C>T	XP_011543020.1:n.1488+12C>T
XM_011544719.1:c.1488+12C>T	XP_011543021.1:n.1488+12C>T
XM_011544720.1:c.1173+12C>T	XP_011543022.1:n.1173+12C>T
XM_011544721.1:c.1173+12C>T	XP_011543023.1:n.1173+12C>T
XM_011544722.1:c.1173+12C>T	XP_011543024.1:n.1173+12C>T
XM_011544723.1:c.1173+12C>T	XP_011543025.1:n.1173+12C>T
XM_011544724.1:c.1173+12C>T	XP_011543026.1:n.1173+12C>T
XM_011544725.1:c.738+12C>T	XP_011543027.1:n.738+12C>T
NM_001318398.1:c.738+12C>T	NP_001305327.1:n.738+12C>T
XM_005273707.4:c.1488+12C>T	XP_005273764.3:n.1488+12C>T
XM_011544718.2:c.1488+12C>T	XP_011543020.1:n.1488+12C>T
XM_011544720.2:c.1173+12C>T	XP_011543022.1:n.1173+12C>T
XM_011544722.2:c.1173+12C>T	XP_011543024.1:n.1173+12C>T
XM_011544723.3:c.1173+12C>T	XP_011543025.1:n.1173+12C>T
XM_011544725.2:c.738+12C>T	XP_011543027.1:n.738+12C>T
XM_017017082.2:c.2037+12C>T	XP_016872571.1:n.2037+12C>T
XM_017017083.2:c.2037+12C>T	XP_016872572.1:n.2037+12C>T
XM_017017084.2:c.1173+12C>T	XP_016872573.1:n.1173+12C>T
XM_017017085.2:c.996+12C>T	XP_016872574.1:n.996+12C>T
XM_017017086.1:c.738+12C>T	XP_016872575.1:n.738+12C>T
NM_001098671.2:c.1173+12C>T MANE Select	NP_001092141.1:n.1173+12C>T
NM_001098670.2:c.1173+12C>T	NP_001092140.1:n.1173+12C>T
NM_001318398.2:c.738+12C>T	NP_001305327.1:n.738+12C>T