Canonical Allele Identifier: CA381583729

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047693-G-A
• MyVariant Identifiers: chr11:g.67815160G>A (hg19) ; chr11:g.68047693G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047693G>A , CM000673.2:g.68047693G>A	GRCh38
NC_000011.9:g.67815160G>A , CM000673.1:g.67815160G>A	GRCh37
NC_000011.8:g.67571736G>A	NCBI36
NG_007878.1:g.13678G>A , LRG_115:g.13678G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.881G>A	ENSP00000513629.1:p.Gly294Asp
ENST00000698255.1:c.1301G>A	ENSP00000513630.1:p.Gly434Asp
ENST00000698256.1:c.818G>A
ENST00000698257.1:n.770G>A
ENST00000698258.1:n.410G>A
ENST00000698259.1:n.176G>A
ENST00000265686.8:c.1352G>A MANE Select	ENSP00000265686.3:p.Gly451Asp
ENST00000265686.7:c.1352G>A	ENSP00000265686.3:p.Gly451Asp
ENST00000525516.1:n.146G>A
ENST00000525724.5:n.664G>A
ENST00000528981.5:c.504G>A
ENST00000529364.1:c.763G>A
ENST00000532635.5:c.704G>A	ENSP00000434407.1:p.Gly235Asp
ENST00000533005.5:n.388G>A
NM_006019.3:c.1352G>A	NP_006010.2:p.Gly451Asp
NM_006053.3:c.704G>A	NP_006044.1:p.Gly235Asp
XM_005273709.2:c.1352G>A	XP_005273766.1:p.Gly451Asp
XM_011544726.1:c.1352G>A	XP_011543028.1:p.Gly451Asp
XM_011544727.1:c.1352G>A	XP_011543029.1:p.Gly451Asp
XM_011544728.1:c.1352G>A	XP_011543030.1:p.Gly451Asp
XM_011544729.1:c.1368G>A	XP_011543031.1:p.Gly456=
XR_949754.1:n.1356G>A
NM_001351059.1:c.458G>A	NP_001337988.1:p.Gly153Asp
XM_024448320.1:c.1368G>A	XP_024304088.1:p.Gly456=
XM_024448321.1:c.1368G>A	XP_024304089.1:p.Gly456=
XM_024448322.1:c.1368G>A	XP_024304090.1:p.Gly456=
XM_024448323.1:c.1368G>A	XP_024304091.1:p.Gly456=
XM_024448324.1:c.1368G>A	XP_024304092.1:p.Gly456=
XR_001747721.2:n.1476G>A
XR_001747722.1:n.1489G>A
XR_001747723.2:n.1489G>A
XR_002957115.1:n.1490G>A
NM_006019.4:c.1352G>A MANE Select	NP_006010.2:p.Gly451Asp
NM_001351059.2:c.458G>A	NP_001337988.1:p.Gly153Asp
NM_006053.4:c.704G>A	NP_006044.1:p.Gly235Asp