Canonical Allele Identifier: CA2658575780

Gene: RASGRP3

Linked Data

• gnomAD v4: 2-33458060-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33458061del , CM000664.2:g.33458061del	GRCh38
NC_000002.11:g.33683128del , CM000664.1:g.33683128del	GRCh37
NC_000002.10:g.33536632del	NCBI36
NG_053077.1:g.26714del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402538.7:c.-261+10118del	ENSP00000385886.3:n.-261+10118del
ENST00000437184.5:c.-330del	ENSP00000393866.1:n.-330del
ENST00000479528.5:n.149+10118del
ENST00000484909.5:n.390+10118del
ENST00000497723.6:n.303+10118del
NM_170672.2:c.-261+10118del	NP_733772.1:n.-261+10118del
XM_011532746.1:c.-159+10118del	XP_011531048.1:n.-159+10118del
NM_001349975.1:c.-383+10118del	NP_001336904.1:n.-383+10118del
NM_001349978.1:c.-261+10118del	NP_001336907.1:n.-261+10118del
NM_001349979.1:c.-330del	NP_001336908.1:n.-330del
XM_011532746.3:c.-159+10118del	XP_011531048.1:n.-159+10118del
XM_011532748.3:c.-330del	XP_011531050.2:n.-330del
XM_017003759.2:c.-1635+10118del	XP_016859248.1:n.-1635+10118del
NM_001349975.2:c.-383+10118del	NP_001336904.1:n.-383+10118del
NM_001349978.2:c.-261+10118del	NP_001336907.1:n.-261+10118del
NM_001349979.2:c.-330del	NP_001336908.1:n.-330del
NM_170672.3:c.-261+10118del	NP_733772.1:n.-261+10118del