Canonical Allele Identifier: CA2614700385

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047850-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047851del , CM000673.2:g.68047851del	GRCh38
NC_000011.9:g.67815318del , CM000673.1:g.67815318del	GRCh37
NC_000011.8:g.67571894del	NCBI36
NG_007878.1:g.13836del , LRG_115:g.13836del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.89-31del
ENST00000698254.1:c.993-31del	ENSP00000513629.1:n.993-31del
ENST00000698255.1:c.1413-31del	ENSP00000513630.1:n.1413-31del
ENST00000698256.1:c.930-31del
ENST00000698257.1:n.882-31del
ENST00000698258.1:n.568del
ENST00000698259.1:n.334del
ENST00000265686.8:c.1464-31del MANE Select	ENSP00000265686.3:n.1464-31del
ENST00000265686.7:c.1464-31del	ENSP00000265686.3:n.1464-31del
ENST00000525516.1:n.258-31del
ENST00000525724.5:n.776-31del
ENST00000528981.5:c.616-31del
ENST00000532635.5:c.816-31del	ENSP00000434407.1:n.816-31del
ENST00000533005.5:n.546del
NM_006019.3:c.1464-31del	NP_006010.2:n.1464-31del
NM_006053.3:c.816-31del	NP_006044.1:n.816-31del
XM_005273709.2:c.1464-31del	XP_005273766.1:n.1464-31del
XM_011544726.1:c.1464-31del	XP_011543028.1:n.1464-31del
XM_011544727.1:c.1464-31del	XP_011543029.1:n.1464-31del
XM_011544728.1:c.1464-31del	XP_011543030.1:n.1464-31del
XM_011544729.1:c.1480-31del	XP_011543031.1:n.1480-31del
XR_949754.1:n.1468-31del
NM_001351059.1:c.570-31del	NP_001337988.1:n.570-31del
XM_024448320.1:c.1526del	XP_024304088.1:p.Ser509ThrfsTer?
XM_024448321.1:c.1526del	XP_024304089.1:p.Ser509ThrfsTer?
XM_024448322.1:c.1526del	XP_024304090.1:p.Ser509ThrfsTer?
XM_024448323.1:c.1526del	XP_024304091.1:p.Ser509ThrfsTer?
XM_024448324.1:c.1526del	XP_024304092.1:p.Ser509ThrfsTer?
XR_001747721.2:n.1588-31del
XR_001747722.1:n.1601-31del
XR_001747723.2:n.1601-31del
XR_002957115.1:n.1648del
NM_006019.4:c.1464-31del MANE Select	NP_006010.2:n.1464-31del
NM_001351059.2:c.570-31del	NP_001337988.1:n.570-31del
NM_006053.4:c.816-31del	NP_006044.1:n.816-31del