Canonical Allele Identifier: CA1243165104

Gene: RASGRP3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33458088_33458089delinsCT , CM000664.2:g.33458088_33458089delinsCT	GRCh38
NC_000002.11:g.33683155_33683156delinsCT , CM000664.1:g.33683155_33683156delinsCT	GRCh37
NC_000002.10:g.33536659_33536660delinsCT	NCBI36
NG_053077.1:g.26741_26742delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402538.7:c.-261+10145_-261+10146delinsCT	ENSP00000385886.3:n.-261+10145_-261+10146delinsCT
ENST00000437184.5:c.-303_-302delinsCT	ENSP00000393866.1:n.-303_-302delinsCT
ENST00000479528.5:n.149+10145_149+10146delinsCT
ENST00000484909.5:n.390+10145_390+10146delinsCT
ENST00000497723.6:n.303+10145_303+10146delinsCT
NM_170672.2:c.-261+10145_-261+10146delinsCT	NP_733772.1:n.-261+10145_-261+10146delinsCT
XM_011532746.1:c.-159+10145_-159+10146delinsCT	XP_011531048.1:n.-159+10145_-159+10146delinsCT
NM_001349975.1:c.-383+10145_-383+10146delinsCT	NP_001336904.1:n.-383+10145_-383+10146delinsCT
NM_001349978.1:c.-261+10145_-261+10146delinsCT	NP_001336907.1:n.-261+10145_-261+10146delinsCT
NM_001349979.1:c.-303_-302delinsCT	NP_001336908.1:n.-303_-302delinsCT
XM_011532746.3:c.-159+10145_-159+10146delinsCT	XP_011531048.1:n.-159+10145_-159+10146delinsCT
XM_011532748.3:c.-303_-302delinsCT	XP_011531050.2:n.-303_-302delinsCT
XM_017003759.2:c.-1635+10145_-1635+10146delinsCT	XP_016859248.1:n.-1635+10145_-1635+10146delinsCT
NM_001349975.2:c.-383+10145_-383+10146delinsCT	NP_001336904.1:n.-383+10145_-383+10146delinsCT
NM_001349978.2:c.-261+10145_-261+10146delinsCT	NP_001336907.1:n.-261+10145_-261+10146delinsCT
NM_001349979.2:c.-303_-302delinsCT	NP_001336908.1:n.-303_-302delinsCT
NM_170672.3:c.-261+10145_-261+10146delinsCT	NP_733772.1:n.-261+10145_-261+10146delinsCT