Canonical Allele Identifier: CA1243164650

Gene: RASGRP3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33457612_33457614delinsGAT , CM000664.2:g.33457612_33457614delinsGAT	GRCh38
NC_000002.11:g.33682679_33682681delinsGAT , CM000664.1:g.33682679_33682681delinsGAT	GRCh37
NC_000002.10:g.33536183_33536185delinsGAT	NCBI36
NG_053077.1:g.26265_26267delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402538.7:c.-261+9669_-261+9671delinsGAT	ENSP00000385886.3:n.-261+9669_-261+9671delinsGAT
ENST00000479528.5:n.149+9669_149+9671delinsGAT
ENST00000484909.5:n.390+9669_390+9671delinsGAT
ENST00000497723.6:n.303+9669_303+9671delinsGAT
NM_170672.2:c.-261+9669_-261+9671delinsGAT	NP_733772.1:n.-261+9669_-261+9671delinsGAT
XM_011532746.1:c.-159+9669_-159+9671delinsGAT	XP_011531048.1:n.-159+9669_-159+9671delinsGAT
NM_001349975.1:c.-383+9669_-383+9671delinsGAT	NP_001336904.1:n.-383+9669_-383+9671delinsGAT
NM_001349978.1:c.-261+9669_-261+9671delinsGAT	NP_001336907.1:n.-261+9669_-261+9671delinsGAT
XM_011532746.3:c.-159+9669_-159+9671delinsGAT	XP_011531048.1:n.-159+9669_-159+9671delinsGAT
XM_017003759.2:c.-1635+9669_-1635+9671delinsGAT	XP_016859248.1:n.-1635+9669_-1635+9671delinsGAT
NM_001349975.2:c.-383+9669_-383+9671delinsGAT	NP_001336904.1:n.-383+9669_-383+9671delinsGAT
NM_001349978.2:c.-261+9669_-261+9671delinsGAT	NP_001336907.1:n.-261+9669_-261+9671delinsGAT
NM_170672.3:c.-261+9669_-261+9671delinsGAT	NP_733772.1:n.-261+9669_-261+9671delinsGAT