Canonical Allele Identifier: CA44892217

Gene: RASGRP3

Linked Data

• dbSNP Id: rs952005806
• gnomAD v3: 2-33458088-CT-C
• gnomAD v4: 2-33458088-CT-C
• MyVariant Identifiers: chr2:g.33683156del (hg19) ; chr2:g.33458089del (hg38)

Genomic Alleles

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

Transcript Alleles

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