Canonical Allele Identifier: CA1243164764

Gene: RASGRP3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33457746_33457750delinsCTGAT , CM000664.2:g.33457746_33457750delinsCTGAT	GRCh38
NC_000002.11:g.33682813_33682817delinsCTGAT , CM000664.1:g.33682813_33682817delinsCTGAT	GRCh37
NC_000002.10:g.33536317_33536321delinsCTGAT	NCBI36
NG_053077.1:g.26399_26403delinsCTGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402538.7:c.-261+9803_-261+9807delinsCTGAT	ENSP00000385886.3:n.-261+9803_-261+9807delinsCTGAT
ENST00000479528.5:n.149+9803_149+9807delinsCTGAT
ENST00000484909.5:n.390+9803_390+9807delinsCTGAT
ENST00000497723.6:n.303+9803_303+9807delinsCTGAT
NM_170672.2:c.-261+9803_-261+9807delinsCTGAT	NP_733772.1:n.-261+9803_-261+9807delinsCTGAT
XM_011532746.1:c.-159+9803_-159+9807delinsCTGAT	XP_011531048.1:n.-159+9803_-159+9807delinsCTGAT
NM_001349975.1:c.-383+9803_-383+9807delinsCTGAT	NP_001336904.1:n.-383+9803_-383+9807delinsCTGAT
NM_001349978.1:c.-261+9803_-261+9807delinsCTGAT	NP_001336907.1:n.-261+9803_-261+9807delinsCTGAT
XM_011532746.3:c.-159+9803_-159+9807delinsCTGAT	XP_011531048.1:n.-159+9803_-159+9807delinsCTGAT
XM_017003759.2:c.-1635+9803_-1635+9807delinsCTGAT	XP_016859248.1:n.-1635+9803_-1635+9807delinsCTGAT
NM_001349975.2:c.-383+9803_-383+9807delinsCTGAT	NP_001336904.1:n.-383+9803_-383+9807delinsCTGAT
NM_001349978.2:c.-261+9803_-261+9807delinsCTGAT	NP_001336907.1:n.-261+9803_-261+9807delinsCTGAT
NM_170672.3:c.-261+9803_-261+9807delinsCTGAT	NP_733772.1:n.-261+9803_-261+9807delinsCTGAT