Canonical Allele Identifier: CA1029131576
Gene: RASGRP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.33457670_33457671insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT , CM000664.2:g.33457670_33457671insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT GRCh38
NC_000002.11:g.33682737_33682738insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT , CM000664.1:g.33682737_33682738insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT GRCh37
NC_000002.10:g.33536241_33536242insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT NCBI36
NG_053077.1:g.26323_26324insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000402538.7:c.-261+9727_-261+9728insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT ENSP00000385886.3:n.-261+9727_-261+9728insTATTCCTCATTTGTGAAAG...
ENST00000479528.5:n.149+9727_149+9728insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT
ENST00000484909.5:n.390+9727_390+9728insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT
ENST00000497723.6:n.303+9727_303+9728insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT
NM_170672.2:c.-261+9727_-261+9728insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT NP_733772.1:n.-261+9727_-261+9728insTATTCCTCATTTGTGAAAGGGAAAT...
XM_011532746.1:c.-159+9727_-159+9728insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT XP_011531048.1:n.-159+9727_-159+9728insTATTCCTCATTTGTGAAAGGGA...
NM_001349975.1:c.-383+9727_-383+9728insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT NP_001336904.1:n.-383+9727_-383+9728insTATTCCTCATTTGTGAAAGGGA...
NM_001349978.1:c.-261+9727_-261+9728insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT NP_001336907.1:n.-261+9727_-261+9728insTATTCCTCATTTGTGAAAGGGA...
XM_011532746.3:c.-159+9727_-159+9728insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT XP_011531048.1:n.-159+9727_-159+9728insTATTCCTCATTTGTGAAAGGGA...
XM_017003759.2:c.-1635+9727_-1635+9728insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT XP_016859248.1:n.-1635+9727_-1635+9728insTATTCCTCATTTGTGAAAGG...
NM_001349975.2:c.-383+9727_-383+9728insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT NP_001336904.1:n.-383+9727_-383+9728insTATTCCTCATTTGTGAAAGGGA...
NM_001349978.2:c.-261+9727_-261+9728insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT NP_001336907.1:n.-261+9727_-261+9728insTATTCCTCATTTGTGAAAGGGA...
NM_170672.3:c.-261+9727_-261+9728insTATTCCTCATTTGTGAAAGGGAAATGATAATACACAACTCAACCCTCACTGCCACCCTTTGAGTTGT NP_733772.1:n.-261+9727_-261+9728insTATTCCTCATTTGTGAAAGGGAAAT...