Canonical Allele Identifier: CA381584181

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815240G>T (hg19) ; chr11:g.68047773G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047773G>T , CM000673.2:g.68047773G>T	GRCh38
NC_000011.9:g.67815240G>T , CM000673.1:g.67815240G>T	GRCh37
NC_000011.8:g.67571816G>T	NCBI36
NG_007878.1:g.13758G>T , LRG_115:g.13758G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.57G>T
ENST00000698254.1:c.961G>T	ENSP00000513629.1:p.Val321Leu
ENST00000698255.1:c.1381G>T	ENSP00000513630.1:p.Val461Leu
ENST00000698256.1:c.898G>T
ENST00000698257.1:n.850G>T
ENST00000698258.1:n.490G>T
ENST00000698259.1:n.256G>T
ENST00000265686.8:c.1432G>T MANE Select	ENSP00000265686.3:p.Val478Leu
ENST00000265686.7:c.1432G>T	ENSP00000265686.3:p.Val478Leu
ENST00000525516.1:n.226G>T
ENST00000525724.5:n.744G>T
ENST00000528981.5:c.584G>T
ENST00000529364.1:c.843G>T
ENST00000532635.5:c.784G>T	ENSP00000434407.1:p.Val262Leu
ENST00000533005.5:n.468G>T
NM_006019.3:c.1432G>T	NP_006010.2:p.Val478Leu
NM_006053.3:c.784G>T	NP_006044.1:p.Val262Leu
XM_005273709.2:c.1432G>T	XP_005273766.1:p.Val478Leu
XM_011544726.1:c.1432G>T	XP_011543028.1:p.Val478Leu
XM_011544727.1:c.1432G>T	XP_011543029.1:p.Val478Leu
XM_011544728.1:c.1432G>T	XP_011543030.1:p.Val478Leu
XM_011544729.1:c.1448G>T	XP_011543031.1:p.Cys483Phe
XR_949754.1:n.1436G>T
NM_001351059.1:c.538G>T	NP_001337988.1:p.Val180Leu
XM_024448320.1:c.1448G>T	XP_024304088.1:p.Cys483Phe
XM_024448321.1:c.1448G>T	XP_024304089.1:p.Cys483Phe
XM_024448322.1:c.1448G>T	XP_024304090.1:p.Cys483Phe
XM_024448323.1:c.1448G>T	XP_024304091.1:p.Cys483Phe
XM_024448324.1:c.1448G>T	XP_024304092.1:p.Cys483Phe
XR_001747721.2:n.1556G>T
XR_001747722.1:n.1569G>T
XR_001747723.2:n.1569G>T
XR_002957115.1:n.1570G>T
NM_006019.4:c.1432G>T MANE Select	NP_006010.2:p.Val478Leu
NM_001351059.2:c.538G>T	NP_001337988.1:p.Val180Leu
NM_006053.4:c.784G>T	NP_006044.1:p.Val262Leu