Canonical Allele Identifier: CA2695214872

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047773_68047790delinsT , CM000673.2:g.68047773_68047790delinsT	GRCh38
NC_000011.9:g.67815240_67815257delinsT , CM000673.1:g.67815240_67815257delinsT	GRCh37
NC_000011.8:g.67571816_67571833delinsT	NCBI36
NG_007878.1:g.13758_13775delinsT , LRG_115:g.13758_13775delinsT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.57_74delinsT
ENST00000698254.1:c.961_978delinsT	ENSP00000513629.1:p.Val321SerfsTer6
ENST00000698255.1:c.1381_1398delinsT	ENSP00000513630.1:p.Val461SerfsTer6
ENST00000698256.1:c.898_915delinsT
ENST00000698257.1:n.850_867delinsT
ENST00000698258.1:n.490_507delinsT
ENST00000698259.1:n.256_273delinsT
ENST00000265686.8:c.1432_1449delinsT MANE Select	ENSP00000265686.3:p.Val478SerfsTer6
ENST00000265686.7:c.1432_1449delinsT	ENSP00000265686.3:p.Val478SerfsTer6
ENST00000525516.1:n.226_243delinsT
ENST00000525724.5:n.744_761delinsT
ENST00000528981.5:c.584_601delinsT
ENST00000529364.1:c.843_860delinsT
ENST00000532635.5:c.784_801delinsT	ENSP00000434407.1:p.Val262SerfsTer6
ENST00000533005.5:n.468_485delinsT
NM_006019.3:c.1432_1449delinsT	NP_006010.2:p.Val478SerfsTer6
NM_006053.3:c.784_801delinsT	NP_006044.1:p.Val262SerfsTer6
XM_005273709.2:c.1432_1449delinsT	XP_005273766.1:p.Val478SerfsTer6
XM_011544726.1:c.1432_1449delinsT	XP_011543028.1:p.Val478SerfsTer6
XM_011544727.1:c.1432_1449delinsT	XP_011543029.1:p.Val478SerfsTer6
XM_011544728.1:c.1432_1449delinsT	XP_011543030.1:p.Val478SerfsTer6
XM_011544729.1:c.1448_1465delinsT	XP_011543031.1:p.Cys483PhefsTer?
XR_949754.1:n.1436_1453delinsT
NM_001351059.1:c.538_555delinsT	NP_001337988.1:p.Val180SerfsTer6
XM_024448320.1:c.1448_1465delinsT	XP_024304088.1:p.Cys483PhefsTer23
XM_024448321.1:c.1448_1465delinsT	XP_024304089.1:p.Cys483PhefsTer23
XM_024448322.1:c.1448_1465delinsT	XP_024304090.1:p.Cys483PhefsTer23
XM_024448323.1:c.1448_1465delinsT	XP_024304091.1:p.Cys483PhefsTer23
XM_024448324.1:c.1448_1465delinsT	XP_024304092.1:p.Cys483PhefsTer23
XR_001747721.2:n.1556_1573delinsT
XR_001747722.1:n.1569_1586delinsT
XR_001747723.2:n.1569_1586delinsT
XR_002957115.1:n.1570_1587delinsT
NM_006019.4:c.1432_1449delinsT MANE Select	NP_006010.2:p.Val478SerfsTer6
NM_001351059.2:c.538_555delinsT	NP_001337988.1:p.Val180SerfsTer6
NM_006053.4:c.784_801delinsT	NP_006044.1:p.Val262SerfsTer6