Canonical Allele Identifier: CA44892218

Gene: RASGRP3

Linked Data

• dbSNP Id: rs952005806
• gnomAD v2: 2-33683155-C-CT
• gnomAD v3: 2-33458088-C-CT
• gnomAD v4: 2-33458088-C-CT
• MyVariant Identifiers: chr2:g.33683155_33683156insT (hg19) ; chr2:g.33458088_33458089insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33458096dup , CM000664.2:g.33458096dup	GRCh38
NC_000002.11:g.33683163dup , CM000664.1:g.33683163dup	GRCh37
NC_000002.10:g.33536667dup	NCBI36
NG_053077.1:g.26749dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402538.7:c.-261+10153dup	ENSP00000385886.3:n.-261+10153dup
ENST00000437184.5:c.-295dup	ENSP00000393866.1:n.-295dup
ENST00000479528.5:n.149+10153dup
ENST00000484909.5:n.390+10153dup
ENST00000497723.6:n.303+10153dup
NM_170672.2:c.-261+10153dup	NP_733772.1:n.-261+10153dup
XM_011532746.1:c.-159+10153dup	XP_011531048.1:n.-159+10153dup
NM_001349975.1:c.-383+10153dup	NP_001336904.1:n.-383+10153dup
NM_001349978.1:c.-261+10153dup	NP_001336907.1:n.-261+10153dup
NM_001349979.1:c.-295dup	NP_001336908.1:n.-295dup
XM_011532746.3:c.-159+10153dup	XP_011531048.1:n.-159+10153dup
XM_011532748.3:c.-295dup	XP_011531050.2:n.-295dup
XM_017003759.2:c.-1635+10153dup	XP_016859248.1:n.-1635+10153dup
NM_001349975.2:c.-383+10153dup	NP_001336904.1:n.-383+10153dup
NM_001349978.2:c.-261+10153dup	NP_001336907.1:n.-261+10153dup
NM_001349979.2:c.-295dup	NP_001336908.1:n.-295dup
NM_170672.3:c.-261+10153dup	NP_733772.1:n.-261+10153dup