Canonical Allele Identifier: CA2614700372

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047831-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047831G>A , CM000673.2:g.68047831G>A	GRCh38
NC_000011.9:g.67815298G>A , CM000673.1:g.67815298G>A	GRCh37
NC_000011.8:g.67571874G>A	NCBI36
NG_007878.1:g.13816G>A , LRG_115:g.13816G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.88+27G>A
ENST00000698254.1:c.992+27G>A	ENSP00000513629.1:n.992+27G>A
ENST00000698255.1:c.1412+27G>A	ENSP00000513630.1:n.1412+27G>A
ENST00000698256.1:c.929+27G>A
ENST00000698257.1:n.881+27G>A
ENST00000698258.1:n.548G>A
ENST00000698259.1:n.314G>A
ENST00000265686.8:c.1463+27G>A MANE Select	ENSP00000265686.3:n.1463+27G>A
ENST00000265686.7:c.1463+27G>A	ENSP00000265686.3:n.1463+27G>A
ENST00000525516.1:n.257+27G>A
ENST00000525724.5:n.775+27G>A
ENST00000528981.5:c.615+27G>A
ENST00000532635.5:c.815+27G>A	ENSP00000434407.1:n.815+27G>A
ENST00000533005.5:n.526G>A
NM_006019.3:c.1463+27G>A	NP_006010.2:n.1463+27G>A
NM_006053.3:c.815+27G>A	NP_006044.1:n.815+27G>A
XM_005273709.2:c.1463+27G>A	XP_005273766.1:n.1463+27G>A
XM_011544726.1:c.1463+27G>A	XP_011543028.1:n.1463+27G>A
XM_011544727.1:c.1463+27G>A	XP_011543029.1:n.1463+27G>A
XM_011544728.1:c.1463+27G>A	XP_011543030.1:n.1463+27G>A
XM_011544729.1:c.1479+27G>A	XP_011543031.1:n.1479+27G>A
XR_949754.1:n.1467+27G>A
NM_001351059.1:c.569+27G>A	NP_001337988.1:n.569+27G>A
XM_024448320.1:c.1506G>A	XP_024304088.1:p.Trp502Ter
XM_024448321.1:c.1506G>A	XP_024304089.1:p.Trp502Ter
XM_024448322.1:c.1506G>A	XP_024304090.1:p.Trp502Ter
XM_024448323.1:c.1506G>A	XP_024304091.1:p.Trp502Ter
XM_024448324.1:c.1506G>A	XP_024304092.1:p.Trp502Ter
XR_001747721.2:n.1587+27G>A
XR_001747722.1:n.1600+27G>A
XR_001747723.2:n.1600+27G>A
XR_002957115.1:n.1628G>A
NM_006019.4:c.1463+27G>A MANE Select	NP_006010.2:n.1463+27G>A
NM_001351059.2:c.569+27G>A	NP_001337988.1:n.569+27G>A
NM_006053.4:c.815+27G>A	NP_006044.1:n.815+27G>A