Canonical Allele Identifier: CA381578327

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68043498G>T , CM000673.2:g.68043498G>T	GRCh38
NC_000011.9:g.67810965G>T , CM000673.1:g.67810965G>T	GRCh37
NC_000011.8:g.67567541G>T	NCBI36
NG_007878.1:g.9483G>T , LRG_115:g.9483G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.630+1G>T MANE Select	NP_006010.2:n.630+1G>T
ENST00000265686.8:c.630+1G>T MANE Select	ENSP00000265686.3:n.630+1G>T
NM_001351059.1:c.-281+1G>T	NP_001337988.1:n.-281+1G>T
NM_001351059.2:c.-281+1G>T	NP_001337988.1:n.-281+1G>T
NM_006019.3:c.630+1G>T	NP_006010.2:n.630+1G>T
NM_006053.3:c.-19+1G>T	NP_006044.1:n.-19+1G>T
NM_006053.4:c.-19+1G>T	NP_006044.1:n.-19+1G>T
ENST00000265686.7:c.630+1G>T	ENSP00000265686.3:n.630+1G>T
ENST00000524598.5:c.588+1G>T	ENSP00000432846.1:n.588+1G>T
ENST00000527530.1:n.176G>T
ENST00000529364.1:c.130+1G>T
ENST00000529657.1:c.630+1G>T	ENSP00000435023.1:n.630+1G>T
ENST00000532635.5:c.-19+1G>T	ENSP00000434407.1:n.-19+1G>T
ENST00000533947.1:n.936+1G>T
ENST00000534673.5:c.504-73G>T	ENSP00000431174.1:n.504-73G>T
ENST00000698254.1:c.403+649G>T	ENSP00000513629.1:n.403+649G>T
ENST00000698255.1:c.630+1G>T	ENSP00000513630.1:n.630+1G>T
ENST00000698256.1:c.80+1G>T
ENST00000698257.1:n.31+1G>T
XM_005273709.2:c.630+1G>T	XP_005273766.1:n.630+1G>T
XM_011544726.1:c.630+1G>T	XP_011543028.1:n.630+1G>T
XM_011544727.1:c.630+1G>T	XP_011543029.1:n.630+1G>T
XM_011544728.1:c.630+1G>T	XP_011543030.1:n.630+1G>T
XM_011544729.1:c.630+1G>T	XP_011543031.1:n.630+1G>T
XM_024448320.1:c.630+1G>T	XP_024304088.1:n.630+1G>T
XM_024448321.1:c.630+1G>T	XP_024304089.1:n.630+1G>T
XM_024448322.1:c.630+1G>T	XP_024304090.1:n.630+1G>T
XM_024448323.1:c.630+1G>T	XP_024304091.1:n.630+1G>T
XM_024448324.1:c.630+1G>T	XP_024304092.1:n.630+1G>T
XR_001747721.2:n.754+1G>T
XR_001747722.1:n.751+1G>T
XR_001747723.2:n.751+1G>T
XR_002957115.1:n.752+1G>T
XR_949754.1:n.634+1G>T