Canonical Allele Identifier: CA44892041

Gene: RASGRP3

Linked Data

• dbSNP Id: rs907609201
• gnomAD v2: 2-33682907-T-TA
• gnomAD v3: 2-33457840-T-TA
• gnomAD v4: 2-33457840-T-TA
• MyVariant Identifiers: chr2:g.33682908_33682909insA (hg19) ; chr2:g.33682907_33682908insA (hg19) ; chr2:g.33457841_33457842insA (hg38) ; chr2:g.33457840_33457841insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33457847dup , CM000664.2:g.33457847dup	GRCh38
NC_000002.11:g.33682914dup , CM000664.1:g.33682914dup	GRCh37
NC_000002.10:g.33536418dup	NCBI36
NG_053077.1:g.26500dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402538.7:c.-261+9904dup	ENSP00000385886.3:n.-261+9904dup
ENST00000479528.5:n.149+9904dup
ENST00000484909.5:n.390+9904dup
ENST00000497723.6:n.303+9904dup
NM_170672.2:c.-261+9904dup	NP_733772.1:n.-261+9904dup
XM_011532746.1:c.-159+9904dup	XP_011531048.1:n.-159+9904dup
NM_001349975.1:c.-383+9904dup	NP_001336904.1:n.-383+9904dup
NM_001349978.1:c.-261+9904dup	NP_001336907.1:n.-261+9904dup
XM_011532746.3:c.-159+9904dup	XP_011531048.1:n.-159+9904dup
XM_017003759.2:c.-1635+9904dup	XP_016859248.1:n.-1635+9904dup
NM_001349975.2:c.-383+9904dup	NP_001336904.1:n.-383+9904dup
NM_001349978.2:c.-261+9904dup	NP_001336907.1:n.-261+9904dup
NM_170672.3:c.-261+9904dup	NP_733772.1:n.-261+9904dup