Canonical Allele Identifier: CA1243165069

Gene: RASGRP3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33458032C= , CM000664.2:g.33458032C=	GRCh38
NC_000002.11:g.33683099C= , CM000664.1:g.33683099C=	GRCh37
NC_000002.10:g.33536603C=	NCBI36
NG_053077.1:g.26685C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402538.7:c.-261+10089C=	ENSP00000385886.3:n.-261+10089C=
ENST00000479528.5:n.149+10089C=
ENST00000484909.5:n.390+10089C=
ENST00000497723.6:n.303+10089C=
NM_170672.2:c.-261+10089C=	NP_733772.1:n.-261+10089C=
XM_011532746.1:c.-159+10089C=	XP_011531048.1:n.-159+10089C=
NM_001349975.1:c.-383+10089C=	NP_001336904.1:n.-383+10089C=
NM_001349978.1:c.-261+10089C=	NP_001336907.1:n.-261+10089C=
XM_011532746.3:c.-159+10089C=	XP_011531048.1:n.-159+10089C=
XM_011532748.3:c.-359C=	XP_011531050.2:n.-359C=
XM_017003759.2:c.-1635+10089C=	XP_016859248.1:n.-1635+10089C=
NM_001349975.2:c.-383+10089C=	NP_001336904.1:n.-383+10089C=
NM_001349978.2:c.-261+10089C=	NP_001336907.1:n.-261+10089C=
NM_170672.3:c.-261+10089C=	NP_733772.1:n.-261+10089C=