Canonical Allele Identifier: CA14098575

Gene: RASGRP1

Linked Data

• dbSNP Id: rs8035957
• gnomAD v2: 15-38838264-T-C
• gnomAD v3: 15-38546063-T-C
• gnomAD v4: 15-38546063-T-C
• MyVariant Identifiers: chr15:g.38838264T>C (hg19) ; chr15:g.38546063T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38546063T>C , CM000677.2:g.38546063T>C	GRCh38
NC_000015.9:g.38838264T>C , CM000677.1:g.38838264T>C	GRCh37
NC_000015.8:g.36625556T>C	NCBI36
NG_023268.1:g.23744A>G
NG_023268.2:g.23744A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000558418.6:c.76+13758A>G	ENSP00000453905.2:n.76+13758A>G
ENST00000561117.6:c.76+13758A>G	ENSP00000454005.2:n.76+13758A>G
ENST00000697780.1:c.76+13758A>G	ENSP00000513436.1:n.76+13758A>G
ENST00000697781.1:n.302+13758A>G
ENST00000697782.1:c.220+13758A>G	ENSP00000513437.1:n.220+13758A>G
ENST00000697783.1:c.220+13758A>G	ENSP00000513438.1:n.220+13758A>G
ENST00000697784.1:c.76+13758A>G	ENSP00000513439.1:n.76+13758A>G
ENST00000697785.1:c.76+13758A>G	ENSP00000513440.1:n.76+13758A>G
ENST00000697786.1:c.76+13758A>G	ENSP00000513441.1:n.76+13758A>G
ENST00000697788.1:n.242+13758A>G
ENST00000697789.1:n.216+13758A>G
ENST00000310803.10:c.220+13758A>G MANE Select	ENSP00000310244.5:n.220+13758A>G
ENST00000310803.9:c.220+13758A>G	ENSP00000310244.5:n.220+13758A>G
ENST00000414708.6:c.220+13758A>G	ENSP00000413105.2:n.220+13758A>G
ENST00000450598.6:c.220+13758A>G	ENSP00000388540.2:n.220+13758A>G
ENST00000539159.5:c.220+13758A>G	ENSP00000444762.2:n.220+13758A>G
ENST00000558164.5:c.220+13758A>G	ENSP00000454164.1:n.220+13758A>G
ENST00000558418.5:c.76+13758A>G	ENSP00000453905.1:n.76+13758A>G
ENST00000558432.5:c.262+13758A>G	ENSP00000453583.1:n.262+13758A>G
ENST00000559830.5:c.220+13758A>G	ENSP00000452721.1:n.220+13758A>G
ENST00000560929.1:c.76+13758A>G	ENSP00000452892.1:n.76+13758A>G
ENST00000561117.5:c.76+13758A>G	ENSP00000454005.1:n.76+13758A>G
ENST00000561180.5:c.373+13758A>G	ENSP00000452859.1:n.373+13758A>G
NM_001128602.1:c.220+13758A>G	NP_001122074.1:n.220+13758A>G
NM_001306086.1:c.220+13758A>G	NP_001293015.1:n.220+13758A>G
NM_005739.3:c.220+13758A>G	NP_005730.2:n.220+13758A>G
XM_005254114.1:c.220+13758A>G	XP_005254171.1:n.220+13758A>G
XM_011521151.1:c.220+13758A>G	XP_011519453.1:n.220+13758A>G
XM_011521153.1:c.220+13758A>G	XP_011519455.1:n.220+13758A>G
XM_011521154.1:c.220+13758A>G	XP_011519456.1:n.220+13758A>G
XR_931740.1:n.398+13758A>G
XM_005254114.3:c.220+13758A>G	XP_005254171.1:n.220+13758A>G
XM_011521151.3:c.220+13758A>G	XP_011519453.1:n.220+13758A>G
XM_017021860.1:c.76+13758A>G	XP_016877349.1:n.76+13758A>G
NM_005739.4:c.220+13758A>G MANE Select	NP_005730.2:n.220+13758A>G
NM_001128602.2:c.220+13758A>G	NP_001122074.1:n.220+13758A>G
NM_001306086.2:c.220+13758A>G	NP_001293015.1:n.220+13758A>G