Canonical Allele Identifier: CA1243165077

Gene: RASGRP3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33458040G= , CM000664.2:g.33458040G=	GRCh38
NC_000002.11:g.33683107G= , CM000664.1:g.33683107G=	GRCh37
NC_000002.10:g.33536611G=	NCBI36
NG_053077.1:g.26693G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402538.7:c.-261+10097G=	ENSP00000385886.3:n.-261+10097G=
ENST00000479528.5:n.149+10097G=
ENST00000484909.5:n.390+10097G=
ENST00000497723.6:n.303+10097G=
NM_170672.2:c.-261+10097G=	NP_733772.1:n.-261+10097G=
XM_011532746.1:c.-159+10097G=	XP_011531048.1:n.-159+10097G=
NM_001349975.1:c.-383+10097G=	NP_001336904.1:n.-383+10097G=
NM_001349978.1:c.-261+10097G=	NP_001336907.1:n.-261+10097G=
XM_011532746.3:c.-159+10097G=	XP_011531048.1:n.-159+10097G=
XM_011532748.3:c.-351G=	XP_011531050.2:n.-351G=
XM_017003759.2:c.-1635+10097G=	XP_016859248.1:n.-1635+10097G=
NM_001349975.2:c.-383+10097G=	NP_001336904.1:n.-383+10097G=
NM_001349978.2:c.-261+10097G=	NP_001336907.1:n.-261+10097G=
NM_170672.3:c.-261+10097G=	NP_733772.1:n.-261+10097G=