Canonical Allele Identifier: CA2792528568

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047706_68047707insACACACCCCAAACACACCCAA , CM000673.2:g.68047706_68047707insACACACCCCAAACACACCCAA	GRCh38
NC_000011.9:g.67815173_67815174insACACACCCCAAACACACCCAA , CM000673.1:g.67815173_67815174insACACACCCCAAACACACCCAA	GRCh37
NC_000011.8:g.67571749_67571750insACACACCCCAAACACACCCAA	NCBI36
NG_007878.1:g.13691_13692insACACACCCCAAACACACCCAA , LRG_115:g.13691_13692insACACACCCCAAACACACCCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.894_895insACACACCCCAAACACACCCAA	ENSP00000513629.1:p.Ile298_Tyr299insThrHisProLysHisThrGln
ENST00000698255.1:c.1314_1315insACACACCCCAAACACACCCAA	ENSP00000513630.1:p.Ile438_Tyr439insThrHisProLysHisThrGln
ENST00000698256.1:c.831_832insACACACCCCAAACACACCCAA
ENST00000698257.1:n.783_784insACACACCCCAAACACACCCAA
ENST00000698258.1:n.423_424insACACACCCCAAACACACCCAA
ENST00000698259.1:n.189_190insACACACCCCAAACACACCCAA
ENST00000265686.8:c.1365_1366insACACACCCCAAACACACCCAA MANE Select	ENSP00000265686.3:p.Ile455_Tyr456insThrHisProLysHisThrGln
ENST00000265686.7:c.1365_1366insACACACCCCAAACACACCCAA	ENSP00000265686.3:p.Ile455_Tyr456insThrHisProLysHisThrGln
ENST00000525516.1:n.159_160insACACACCCCAAACACACCCAA
ENST00000525724.5:n.677_678insACACACCCCAAACACACCCAA
ENST00000528981.5:c.517_518insACACACCCCAAACACACCCAA
ENST00000529364.1:c.776_777insACACACCCCAAACACACCCAA
ENST00000532635.5:c.717_718insACACACCCCAAACACACCCAA	ENSP00000434407.1:p.Ile239_Tyr240insThrHisProLysHisThrGln
ENST00000533005.5:n.401_402insACACACCCCAAACACACCCAA
NM_006019.3:c.1365_1366insACACACCCCAAACACACCCAA	NP_006010.2:p.Ile455_Tyr456insThrHisProLysHisThrGln
NM_006053.3:c.717_718insACACACCCCAAACACACCCAA	NP_006044.1:p.Ile239_Tyr240insThrHisProLysHisThrGln
XM_005273709.2:c.1365_1366insACACACCCCAAACACACCCAA	XP_005273766.1:p.Ile455_Tyr456insThrHisProLysHisThrGln
XM_011544726.1:c.1365_1366insACACACCCCAAACACACCCAA	XP_011543028.1:p.Ile455_Tyr456insThrHisProLysHisThrGln
XM_011544727.1:c.1365_1366insACACACCCCAAACACACCCAA	XP_011543029.1:p.Ile455_Tyr456insThrHisProLysHisThrGln
XM_011544728.1:c.1365_1366insACACACCCCAAACACACCCAA	XP_011543030.1:p.Ile455_Tyr456insThrHisProLysHisThrGln
XM_011544729.1:c.1381_1382insACACACCCCAAACACACCCAA	XP_011543031.1:p.Leu461delinsHisThrProGlnThrHisProIle
XR_949754.1:n.1369_1370insACACACCCCAAACACACCCAA
NM_001351059.1:c.471_472insACACACCCCAAACACACCCAA	NP_001337988.1:p.Ile157_Tyr158insThrHisProLysHisThrGln
XM_024448320.1:c.1381_1382insACACACCCCAAACACACCCAA	XP_024304088.1:p.Leu461delinsHisThrProGlnThrHisProIle
XM_024448321.1:c.1381_1382insACACACCCCAAACACACCCAA	XP_024304089.1:p.Leu461delinsHisThrProGlnThrHisProIle
XM_024448322.1:c.1381_1382insACACACCCCAAACACACCCAA	XP_024304090.1:p.Leu461delinsHisThrProGlnThrHisProIle
XM_024448323.1:c.1381_1382insACACACCCCAAACACACCCAA	XP_024304091.1:p.Leu461delinsHisThrProGlnThrHisProIle
XM_024448324.1:c.1381_1382insACACACCCCAAACACACCCAA	XP_024304092.1:p.Leu461delinsHisThrProGlnThrHisProIle
XR_001747721.2:n.1489_1490insACACACCCCAAACACACCCAA
XR_001747722.1:n.1502_1503insACACACCCCAAACACACCCAA
XR_001747723.2:n.1502_1503insACACACCCCAAACACACCCAA
XR_002957115.1:n.1503_1504insACACACCCCAAACACACCCAA
NM_006019.4:c.1365_1366insACACACCCCAAACACACCCAA MANE Select	NP_006010.2:p.Ile455_Tyr456insThrHisProLysHisThrGln
NM_001351059.2:c.471_472insACACACCCCAAACACACCCAA	NP_001337988.1:p.Ile157_Tyr158insThrHisProLysHisThrGln
NM_006053.4:c.717_718insACACACCCCAAACACACCCAA	NP_006044.1:p.Ile239_Tyr240insThrHisProLysHisThrGln