Canonical Allele Identifier: CA381584586

Gene: TCIRG1

Linked Data

• COSMIC: COSM1605129
• MyVariant Identifiers: chr11:g.67815401G>T (hg19) ; chr11:g.68047934G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047934G>T , CM000673.2:g.68047934G>T	GRCh38
NC_000011.9:g.67815401G>T , CM000673.1:g.67815401G>T	GRCh37
NC_000011.8:g.67571977G>T	NCBI36
NG_007878.1:g.13919G>T , LRG_115:g.13919G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.141G>T
ENST00000698254.1:c.1045G>T	ENSP00000513629.1:p.Gly349Cys
ENST00000698255.1:c.1465G>T	ENSP00000513630.1:p.Gly489Cys
ENST00000698256.1:c.982G>T
ENST00000698257.1:n.934G>T
ENST00000698258.1:n.651G>T
ENST00000698259.1:n.417G>T
ENST00000265686.8:c.1516G>T MANE Select	ENSP00000265686.3:p.Gly506Cys
ENST00000265686.7:c.1516G>T	ENSP00000265686.3:p.Gly506Cys
ENST00000525516.1:n.310G>T
ENST00000525724.5:n.828G>T
ENST00000528981.5:c.668G>T
ENST00000532635.5:c.868G>T	ENSP00000434407.1:p.Gly290Cys
ENST00000533005.5:n.629G>T
NM_006019.3:c.1516G>T	NP_006010.2:p.Gly506Cys
NM_006053.3:c.868G>T	NP_006044.1:p.Gly290Cys
XM_005273709.2:c.1516G>T	XP_005273766.1:p.Gly506Cys
XM_011544726.1:c.1516G>T	XP_011543028.1:p.Gly506Cys
XM_011544727.1:c.1516G>T	XP_011543029.1:p.Gly506Cys
XM_011544728.1:c.1516G>T	XP_011543030.1:p.Gly506Cys
XR_949754.1:n.1520G>T
NM_001351059.1:c.622G>T	NP_001337988.1:p.Gly208Cys
XM_024448320.1:c.1609G>T	XP_024304088.1:p.Gly537Cys
XM_024448321.1:c.1609G>T	XP_024304089.1:p.Gly537Cys
XM_024448322.1:c.1609G>T	XP_024304090.1:p.Gly537Cys
XM_024448323.1:c.1609G>T	XP_024304091.1:p.Gly537Cys
XM_024448324.1:c.1609G>T	XP_024304092.1:p.Gly537Cys
XR_001747721.2:n.1640G>T
XR_001747722.1:n.1653G>T
XR_001747723.2:n.1653G>T
XR_002957115.1:n.1731G>T
NM_006019.4:c.1516G>T MANE Select	NP_006010.2:p.Gly506Cys
NM_001351059.2:c.622G>T	NP_001337988.1:p.Gly208Cys
NM_006053.4:c.868G>T	NP_006044.1:p.Gly290Cys