Canonical Allele Identifier: CA2749427072
Gene: RASGRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.33458066dup , CM000664.2:g.33458066dup GRCh38
NC_000002.11:g.33683133dup , CM000664.1:g.33683133dup GRCh37
NC_000002.10:g.33536637dup NCBI36
NG_053077.1:g.26719dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000402538.7:c.-261+10123dup ENSP00000385886.3:n.-261+10123dup
ENST00000437184.5:c.-325dup ENSP00000393866.1:n.-325dup
ENST00000479528.5:n.149+10123dup
ENST00000484909.5:n.390+10123dup
ENST00000497723.6:n.303+10123dup
NM_170672.2:c.-261+10123dup NP_733772.1:n.-261+10123dup
XM_011532746.1:c.-159+10123dup XP_011531048.1:n.-159+10123dup
NM_001349975.1:c.-383+10123dup NP_001336904.1:n.-383+10123dup
NM_001349978.1:c.-261+10123dup NP_001336907.1:n.-261+10123dup
NM_001349979.1:c.-325dup NP_001336908.1:n.-325dup
XM_011532746.3:c.-159+10123dup XP_011531048.1:n.-159+10123dup
XM_011532748.3:c.-325dup XP_011531050.2:n.-325dup
XM_017003759.2:c.-1635+10123dup XP_016859248.1:n.-1635+10123dup
NM_001349975.2:c.-383+10123dup NP_001336904.1:n.-383+10123dup
NM_001349978.2:c.-261+10123dup NP_001336907.1:n.-261+10123dup
NM_001349979.2:c.-325dup NP_001336908.1:n.-325dup
NM_170672.3:c.-261+10123dup NP_733772.1:n.-261+10123dup