Canonical Allele Identifier: CA381583966

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815201T>G (hg19) ; chr11:g.68047734T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047734T>G , CM000673.2:g.68047734T>G	GRCh38
NC_000011.9:g.67815201T>G , CM000673.1:g.67815201T>G	GRCh37
NC_000011.8:g.67571777T>G	NCBI36
NG_007878.1:g.13719T>G , LRG_115:g.13719T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.18T>G
ENST00000698254.1:c.922T>G	ENSP00000513629.1:p.Phe308Val
ENST00000698255.1:c.1342T>G	ENSP00000513630.1:p.Phe448Val
ENST00000698256.1:c.859T>G
ENST00000698257.1:n.811T>G
ENST00000698258.1:n.451T>G
ENST00000698259.1:n.217T>G
ENST00000265686.8:c.1393T>G MANE Select	ENSP00000265686.3:p.Phe465Val
ENST00000265686.7:c.1393T>G	ENSP00000265686.3:p.Phe465Val
ENST00000525516.1:n.187T>G
ENST00000525724.5:n.705T>G
ENST00000528981.5:c.545T>G
ENST00000529364.1:c.804T>G
ENST00000532635.5:c.745T>G	ENSP00000434407.1:p.Phe249Val
ENST00000533005.5:n.429T>G
NM_006019.3:c.1393T>G	NP_006010.2:p.Phe465Val
NM_006053.3:c.745T>G	NP_006044.1:p.Phe249Val
XM_005273709.2:c.1393T>G	XP_005273766.1:p.Phe465Val
XM_011544726.1:c.1393T>G	XP_011543028.1:p.Phe465Val
XM_011544727.1:c.1393T>G	XP_011543029.1:p.Phe465Val
XM_011544728.1:c.1393T>G	XP_011543030.1:p.Phe465Val
XM_011544729.1:c.1409T>G	XP_011543031.1:p.Leu470Arg
XR_949754.1:n.1397T>G
NM_001351059.1:c.499T>G	NP_001337988.1:p.Phe167Val
XM_024448320.1:c.1409T>G	XP_024304088.1:p.Leu470Arg
XM_024448321.1:c.1409T>G	XP_024304089.1:p.Leu470Arg
XM_024448322.1:c.1409T>G	XP_024304090.1:p.Leu470Arg
XM_024448323.1:c.1409T>G	XP_024304091.1:p.Leu470Arg
XM_024448324.1:c.1409T>G	XP_024304092.1:p.Leu470Arg
XR_001747721.2:n.1517T>G
XR_001747722.1:n.1530T>G
XR_001747723.2:n.1530T>G
XR_002957115.1:n.1531T>G
NM_006019.4:c.1393T>G MANE Select	NP_006010.2:p.Phe465Val
NM_001351059.2:c.499T>G	NP_001337988.1:p.Phe167Val
NM_006053.4:c.745T>G	NP_006044.1:p.Phe249Val