Canonical Allele Identifier: CA14186672

Gene: RASGRP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38530704T>C , CM000677.2:g.38530704T>C	GRCh38
NC_000015.9:g.38822905T>C , CM000677.1:g.38822905T>C	GRCh37
NC_000015.8:g.36610197T>C	NCBI36
NG_023268.1:g.39103A>G
NG_023268.2:g.39103A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558418.6:c.77-4300A>G	ENSP00000453905.2:n.77-4300A>G
ENST00000561117.6:c.77-4300A>G	ENSP00000454005.2:n.77-4300A>G
ENST00000697780.1:c.77-4300A>G	ENSP00000513436.1:n.77-4300A>G
ENST00000697781.1:n.303-4300A>G
ENST00000697782.1:c.221-4300A>G	ENSP00000513437.1:n.221-4300A>G
ENST00000697783.1:c.221-4300A>G	ENSP00000513438.1:n.221-4300A>G
ENST00000697784.1:c.77-4300A>G	ENSP00000513439.1:n.77-4300A>G
ENST00000697785.1:c.77-4300A>G	ENSP00000513440.1:n.77-4300A>G
ENST00000697786.1:c.77-11327A>G	ENSP00000513441.1:n.77-11327A>G
ENST00000697788.1:n.243-4300A>G
ENST00000697789.1:n.217-4300A>G
ENST00000310803.10:c.221-4300A>G MANE Select	ENSP00000310244.5:n.221-4300A>G
ENST00000310803.9:c.221-4300A>G	ENSP00000310244.5:n.221-4300A>G
ENST00000414708.6:c.221-4300A>G	ENSP00000413105.2:n.221-4300A>G
ENST00000450598.6:c.221-4300A>G	ENSP00000388540.2:n.221-4300A>G
ENST00000539159.5:c.221-4300A>G	ENSP00000444762.2:n.221-4300A>G
ENST00000558164.5:c.221-4300A>G	ENSP00000454164.1:n.221-4300A>G
ENST00000558418.5:c.77-4300A>G	ENSP00000453905.1:n.77-4300A>G
ENST00000558432.5:c.263-4300A>G	ENSP00000453583.1:n.263-4300A>G
ENST00000559830.5:c.221-4300A>G	ENSP00000452721.1:n.221-4300A>G
ENST00000560929.1:c.77-4300A>G	ENSP00000452892.1:n.77-4300A>G
ENST00000561117.5:c.77-4300A>G	ENSP00000454005.1:n.77-4300A>G
ENST00000561180.5:c.374-4300A>G	ENSP00000452859.1:n.374-4300A>G
NM_001128602.1:c.221-4300A>G	NP_001122074.1:n.221-4300A>G
NM_001306086.1:c.221-4300A>G	NP_001293015.1:n.221-4300A>G
NM_005739.3:c.221-4300A>G	NP_005730.2:n.221-4300A>G
XM_005254114.1:c.221-4300A>G	XP_005254171.1:n.221-4300A>G
XM_011521151.1:c.221-4300A>G	XP_011519453.1:n.221-4300A>G
XM_011521153.1:c.221-4300A>G	XP_011519455.1:n.221-4300A>G
XM_011521154.1:c.221-4300A>G	XP_011519456.1:n.221-4300A>G
XR_931740.1:n.399-4300A>G
XM_005254114.3:c.221-4300A>G	XP_005254171.1:n.221-4300A>G
XM_011521151.3:c.221-4300A>G	XP_011519453.1:n.221-4300A>G
XM_017021860.1:c.77-4300A>G	XP_016877349.1:n.77-4300A>G
NM_005739.4:c.221-4300A>G MANE Select	NP_005730.2:n.221-4300A>G
NM_001128602.2:c.221-4300A>G	NP_001122074.1:n.221-4300A>G
NM_001306086.2:c.221-4300A>G	NP_001293015.1:n.221-4300A>G