Canonical Allele Identifier: CA381578374

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68043569A>C , CM000673.2:g.68043569A>C	GRCh38
NC_000011.9:g.67811036A>C , CM000673.1:g.67811036A>C	GRCh37
NC_000011.8:g.67567612A>C	NCBI36
NG_007878.1:g.9554A>C , LRG_115:g.9554A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.631-2A>C MANE Select	NP_006010.2:n.631-2A>C
ENST00000265686.8:c.631-2A>C MANE Select	ENSP00000265686.3:n.631-2A>C
NM_001351059.1:c.-280-2A>C	NP_001337988.1:n.-280-2A>C
NM_001351059.2:c.-280-2A>C	NP_001337988.1:n.-280-2A>C
NM_006019.3:c.631-2A>C	NP_006010.2:n.631-2A>C
NM_006053.3:c.-18-2A>C	NP_006044.1:n.-18-2A>C
NM_006053.4:c.-18-2A>C	NP_006044.1:n.-18-2A>C
ENST00000265686.7:c.631-2A>C	ENSP00000265686.3:n.631-2A>C
ENST00000524598.5:c.589-2A>C	ENSP00000432846.1:n.589-2A>C
ENST00000527530.1:n.247A>C
ENST00000529364.1:c.131-2A>C
ENST00000529657.1:c.631-2A>C	ENSP00000435023.1:n.631-2A>C
ENST00000532635.5:c.-18-2A>C	ENSP00000434407.1:n.-18-2A>C
ENST00000533947.1:n.937-2A>C
ENST00000534673.5:c.504-2A>C	ENSP00000431174.1:n.504-2A>C
ENST00000698254.1:c.404-630A>C	ENSP00000513629.1:n.404-630A>C
ENST00000698255.1:c.631-53A>C	ENSP00000513630.1:n.631-53A>C
ENST00000698256.1:c.81-2A>C
ENST00000698257.1:n.47A>C
XM_005273709.2:c.631-2A>C	XP_005273766.1:n.631-2A>C
XM_011544726.1:c.631-2A>C	XP_011543028.1:n.631-2A>C
XM_011544727.1:c.631-2A>C	XP_011543029.1:n.631-2A>C
XM_011544728.1:c.631-2A>C	XP_011543030.1:n.631-2A>C
XM_011544729.1:c.631-2A>C	XP_011543031.1:n.631-2A>C
XM_024448320.1:c.631-2A>C	XP_024304088.1:n.631-2A>C
XM_024448321.1:c.631-2A>C	XP_024304089.1:n.631-2A>C
XM_024448322.1:c.631-2A>C	XP_024304090.1:n.631-2A>C
XM_024448323.1:c.631-2A>C	XP_024304091.1:n.631-2A>C
XM_024448324.1:c.631-2A>C	XP_024304092.1:n.631-2A>C
XR_001747721.2:n.755-2A>C
XR_001747722.1:n.752-2A>C
XR_001747723.2:n.752-2A>C
XR_002957115.1:n.753-2A>C
XR_949754.1:n.635-2A>C