Canonical Allele Identifier: CA600238439

Gene: TCIRG1

Linked Data

• dbSNP Id: rs1178379709
• gnomAD v2: 11-67815181-GCTT-G
• MyVariant Identifiers: chr11:g.67815182_67815184del (hg19) ; chr11:g.68047715_68047717del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047716_68047718del , CM000673.2:g.68047716_68047718del	GRCh38
NC_000011.9:g.67815183_67815185del , CM000673.1:g.67815183_67815185del	GRCh37
NC_000011.8:g.67571759_67571761del	NCBI36
NG_007878.1:g.13701_13703del , LRG_115:g.13701_13703del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.904_906del	ENSP00000513629.1:p.Phe302del
ENST00000698255.1:c.1324_1326del	ENSP00000513630.1:p.Phe442del
ENST00000698256.1:c.841_843del
ENST00000698257.1:n.793_795del
ENST00000698258.1:n.433_435del
ENST00000698259.1:n.199_201del
ENST00000265686.8:c.1375_1377del MANE Select	ENSP00000265686.3:p.Phe459del
ENST00000265686.7:c.1375_1377del	ENSP00000265686.3:p.Phe459del
ENST00000525516.1:n.169_171del
ENST00000525724.5:n.687_689del
ENST00000528981.5:c.527_529del
ENST00000529364.1:c.786_788del
ENST00000532635.5:c.727_729del	ENSP00000434407.1:p.Phe243del
ENST00000533005.5:n.411_413del
NM_006019.3:c.1375_1377del	NP_006010.2:p.Phe459del
NM_006053.3:c.727_729del	NP_006044.1:p.Phe243del
XM_005273709.2:c.1375_1377del	XP_005273766.1:p.Phe459del
XM_011544726.1:c.1375_1377del	XP_011543028.1:p.Phe459del
XM_011544727.1:c.1375_1377del	XP_011543029.1:p.Phe459del
XM_011544728.1:c.1375_1377del	XP_011543030.1:p.Phe459del
XM_011544729.1:c.1391_1393del	XP_011543031.1:p.Leu464del
XR_949754.1:n.1379_1381del
NM_001351059.1:c.481_483del	NP_001337988.1:p.Phe161del
XM_024448320.1:c.1391_1393del	XP_024304088.1:p.Leu464del
XM_024448321.1:c.1391_1393del	XP_024304089.1:p.Leu464del
XM_024448322.1:c.1391_1393del	XP_024304090.1:p.Leu464del
XM_024448323.1:c.1391_1393del	XP_024304091.1:p.Leu464del
XM_024448324.1:c.1391_1393del	XP_024304092.1:p.Leu464del
XR_001747721.2:n.1499_1501del
XR_001747722.1:n.1512_1514del
XR_001747723.2:n.1512_1514del
XR_002957115.1:n.1513_1515del
NM_006019.4:c.1375_1377del MANE Select	NP_006010.2:p.Phe459del
NM_001351059.2:c.481_483del	NP_001337988.1:p.Phe161del
NM_006053.4:c.727_729del	NP_006044.1:p.Phe243del