Canonical Allele Identifier: CA381584143

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815234T>C (hg19) ; chr11:g.68047767T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047767T>C , CM000673.2:g.68047767T>C	GRCh38
NC_000011.9:g.67815234T>C , CM000673.1:g.67815234T>C	GRCh37
NC_000011.8:g.67571810T>C	NCBI36
NG_007878.1:g.13752T>C , LRG_115:g.13752T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.51T>C
ENST00000698254.1:c.955T>C	ENSP00000513629.1:p.Trp319Arg
ENST00000698255.1:c.1375T>C	ENSP00000513630.1:p.Trp459Arg
ENST00000698256.1:c.892T>C
ENST00000698257.1:n.844T>C
ENST00000698258.1:n.484T>C
ENST00000698259.1:n.250T>C
ENST00000265686.8:c.1426T>C MANE Select	ENSP00000265686.3:p.Trp476Arg
ENST00000265686.7:c.1426T>C	ENSP00000265686.3:p.Trp476Arg
ENST00000525516.1:n.220T>C
ENST00000525724.5:n.738T>C
ENST00000528981.5:c.578T>C
ENST00000529364.1:c.837T>C
ENST00000532635.5:c.778T>C	ENSP00000434407.1:p.Trp260Arg
ENST00000533005.5:n.462T>C
NM_006019.3:c.1426T>C	NP_006010.2:p.Trp476Arg
NM_006053.3:c.778T>C	NP_006044.1:p.Trp260Arg
XM_005273709.2:c.1426T>C	XP_005273766.1:p.Trp476Arg
XM_011544726.1:c.1426T>C	XP_011543028.1:p.Trp476Arg
XM_011544727.1:c.1426T>C	XP_011543029.1:p.Trp476Arg
XM_011544728.1:c.1426T>C	XP_011543030.1:p.Trp476Arg
XM_011544729.1:c.1442T>C	XP_011543031.1:p.Leu481Pro
XR_949754.1:n.1430T>C
NM_001351059.1:c.532T>C	NP_001337988.1:p.Trp178Arg
XM_024448320.1:c.1442T>C	XP_024304088.1:p.Leu481Pro
XM_024448321.1:c.1442T>C	XP_024304089.1:p.Leu481Pro
XM_024448322.1:c.1442T>C	XP_024304090.1:p.Leu481Pro
XM_024448323.1:c.1442T>C	XP_024304091.1:p.Leu481Pro
XM_024448324.1:c.1442T>C	XP_024304092.1:p.Leu481Pro
XR_001747721.2:n.1550T>C
XR_001747722.1:n.1563T>C
XR_001747723.2:n.1563T>C
XR_002957115.1:n.1564T>C
NM_006019.4:c.1426T>C MANE Select	NP_006010.2:p.Trp476Arg
NM_001351059.2:c.532T>C	NP_001337988.1:p.Trp178Arg
NM_006053.4:c.778T>C	NP_006044.1:p.Trp260Arg