Canonical Allele Identifier: CA1243164531
Gene: RASGRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.33457499_33457501delinsATG , CM000664.2:g.33457499_33457501delinsATG GRCh38
NC_000002.11:g.33682566_33682568delinsATG , CM000664.1:g.33682566_33682568delinsATG GRCh37
NC_000002.10:g.33536070_33536072delinsATG NCBI36
NG_053077.1:g.26152_26154delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000402538.7:c.-261+9556_-261+9558delinsATG ENSP00000385886.3:n.-261+9556_-261+9558delinsATG
ENST00000479528.5:n.149+9556_149+9558delinsATG
ENST00000484909.5:n.390+9556_390+9558delinsATG
ENST00000497723.6:n.303+9556_303+9558delinsATG
NM_170672.2:c.-261+9556_-261+9558delinsATG NP_733772.1:n.-261+9556_-261+9558delinsATG
XM_011532746.1:c.-159+9556_-159+9558delinsATG XP_011531048.1:n.-159+9556_-159+9558delinsATG
NM_001349975.1:c.-383+9556_-383+9558delinsATG NP_001336904.1:n.-383+9556_-383+9558delinsATG
NM_001349978.1:c.-261+9556_-261+9558delinsATG NP_001336907.1:n.-261+9556_-261+9558delinsATG
XM_011532746.3:c.-159+9556_-159+9558delinsATG XP_011531048.1:n.-159+9556_-159+9558delinsATG
XM_017003759.2:c.-1635+9556_-1635+9558delinsATG XP_016859248.1:n.-1635+9556_-1635+9558delinsATG
NM_001349975.2:c.-383+9556_-383+9558delinsATG NP_001336904.1:n.-383+9556_-383+9558delinsATG
NM_001349978.2:c.-261+9556_-261+9558delinsATG NP_001336907.1:n.-261+9556_-261+9558delinsATG
NM_170672.3:c.-261+9556_-261+9558delinsATG NP_733772.1:n.-261+9556_-261+9558delinsATG