Canonical Allele Identifier: CA381583502

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815132A>T (hg19) ; chr11:g.68047665A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047665A>T , CM000673.2:g.68047665A>T	GRCh38
NC_000011.9:g.67815132A>T , CM000673.1:g.67815132A>T	GRCh37
NC_000011.8:g.67571708A>T	NCBI36
NG_007878.1:g.13650A>T , LRG_115:g.13650A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.853A>T	ENSP00000513629.1:p.Arg285Trp
ENST00000698255.1:c.1273A>T	ENSP00000513630.1:p.Arg425Trp
ENST00000698256.1:c.790A>T
ENST00000698257.1:n.742A>T
ENST00000698258.1:n.382A>T
ENST00000698259.1:n.148A>T
ENST00000265686.8:c.1324A>T MANE Select	ENSP00000265686.3:p.Arg442Trp
ENST00000265686.7:c.1324A>T	ENSP00000265686.3:p.Arg442Trp
ENST00000525516.1:n.118A>T
ENST00000525724.5:n.636A>T
ENST00000528981.5:c.476A>T
ENST00000529364.1:c.735A>T
ENST00000532635.5:c.676A>T	ENSP00000434407.1:p.Arg226Trp
ENST00000533005.5:n.360A>T
NM_006019.3:c.1324A>T	NP_006010.2:p.Arg442Trp
NM_006053.3:c.676A>T	NP_006044.1:p.Arg226Trp
XM_005273709.2:c.1324A>T	XP_005273766.1:p.Arg442Trp
XM_011544726.1:c.1324A>T	XP_011543028.1:p.Arg442Trp
XM_011544727.1:c.1324A>T	XP_011543029.1:p.Arg442Trp
XM_011544728.1:c.1324A>T	XP_011543030.1:p.Arg442Trp
XM_011544729.1:c.1340A>T	XP_011543031.1:p.Gln447Leu
XR_949754.1:n.1328A>T
NM_001351059.1:c.430A>T	NP_001337988.1:p.Arg144Trp
XM_024448320.1:c.1340A>T	XP_024304088.1:p.Gln447Leu
XM_024448321.1:c.1340A>T	XP_024304089.1:p.Gln447Leu
XM_024448322.1:c.1340A>T	XP_024304090.1:p.Gln447Leu
XM_024448323.1:c.1340A>T	XP_024304091.1:p.Gln447Leu
XM_024448324.1:c.1340A>T	XP_024304092.1:p.Gln447Leu
XR_001747721.2:n.1448A>T
XR_001747722.1:n.1461A>T
XR_001747723.2:n.1461A>T
XR_002957115.1:n.1462A>T
NM_006019.4:c.1324A>T MANE Select	NP_006010.2:p.Arg442Trp
NM_001351059.2:c.430A>T	NP_001337988.1:p.Arg144Trp
NM_006053.4:c.676A>T	NP_006044.1:p.Arg226Trp