Canonical Allele Identifier: CA1243174028

Gene: RASGRP3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33476823T= , CM000664.2:g.33476823T=	GRCh38
NC_000002.11:g.33701890T= , CM000664.1:g.33701890T=	GRCh37
NC_000002.10:g.33555394T=	NCBI36
NG_053077.1:g.45476T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403687.8:c.-261+116T= MANE Select	ENSP00000384192.3:n.-261+116T=
ENST00000402538.7:c.-261+28880T=	ENSP00000385886.3:n.-261+28880T=
ENST00000403687.7:c.-261+116T=	ENSP00000384192.3:n.-261+116T=
ENST00000423159.5:c.-159+116T=	ENSP00000388139.1:n.-159+116T=
ENST00000425210.5:c.-380+116T=	ENSP00000401974.1:n.-380+116T=
ENST00000437184.5:c.-261+18693T=	ENSP00000393866.1:n.-261+18693T=
ENST00000442390.5:c.-281+116T=	ENSP00000405648.1:n.-281+116T=
ENST00000444784.5:c.-159+116T=	ENSP00000400602.1:n.-159+116T=
ENST00000479528.5:n.149+28880T=
ENST00000482857.5:n.111+116T=
ENST00000484909.5:n.391-4360T=
ENST00000494927.1:n.43+116T=
ENST00000497723.6:n.304-4360T=
NM_001139488.1:c.-261+116T=	NP_001132960.1:n.-261+116T=
NM_170672.2:c.-261+28880T=	NP_733772.1:n.-261+28880T=
XM_005264246.2:c.-261+116T=	XP_005264303.1:n.-261+116T=
XM_011532746.1:c.-159+28880T=	XP_011531048.1:n.-159+28880T=
XM_011532747.1:c.-159+116T=	XP_011531049.1:n.-159+116T=
NM_001349975.1:c.-382-4360T=	NP_001336904.1:n.-382-4360T=
NM_001349976.1:c.-159+116T=	NP_001336905.1:n.-159+116T=
NM_001349977.1:c.-383+116T=	NP_001336906.1:n.-383+116T=
NM_001349978.1:c.-261+28880T=	NP_001336907.1:n.-261+28880T=
NM_001349979.1:c.-261+18693T=	NP_001336908.1:n.-261+18693T=
NM_001349980.1:c.-383+116T=	NP_001336909.1:n.-383+116T=
NM_001349981.1:c.-261+116T=	NP_001336910.1:n.-261+116T=
XM_011532746.3:c.-159+28880T=	XP_011531048.1:n.-159+28880T=
XM_011532748.3:c.-261+18693T=	XP_011531050.2:n.-261+18693T=
XM_017003759.2:c.-1634-4360T=	XP_016859248.1:n.-1634-4360T=
XR_001738691.2:n.480+116T=
XR_001738692.2:n.480+116T=
XR_001738693.2:n.480+116T=
NM_001139488.2:c.-261+116T= MANE Select	NP_001132960.1:n.-261+116T=
NM_001349975.2:c.-382-4360T=	NP_001336904.1:n.-382-4360T=
NM_001349976.2:c.-159+116T=	NP_001336905.1:n.-159+116T=
NM_001349977.2:c.-383+116T=	NP_001336906.1:n.-383+116T=
NM_001349978.2:c.-261+28880T=	NP_001336907.1:n.-261+28880T=
NM_001349979.2:c.-261+18693T=	NP_001336908.1:n.-261+18693T=
NM_001349980.2:c.-383+116T=	NP_001336909.1:n.-383+116T=
NM_001349981.2:c.-261+116T=	NP_001336910.1:n.-261+116T=
NM_170672.3:c.-261+28880T=	NP_733772.1:n.-261+28880T=