Canonical Allele Identifier: CA475450251

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67816441G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048974G>T , CM000673.2:g.68048974G>T	GRCh38
NC_000011.9:g.67816441G>T , CM000673.1:g.67816441G>T	GRCh37
NC_000011.8:g.67573017G>T	NCBI36
NG_007878.1:g.14959G>T , LRG_115:g.14959G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.275G>T
ENST00000698254.1:c.1179G>T	ENSP00000513629.1:p.Val393=
ENST00000698255.1:c.1599G>T	ENSP00000513630.1:p.Val533=
ENST00000698256.1:c.1116G>T
ENST00000698257.1:n.1068G>T
ENST00000698258.1:n.785G>T
ENST00000698259.1:n.551G>T
ENST00000265686.8:c.1650G>T MANE Select	ENSP00000265686.3:p.Val550=
ENST00000265686.7:c.1650G>T	ENSP00000265686.3:p.Val550=
ENST00000525724.5:n.962G>T
ENST00000532635.5:c.1002G>T	ENSP00000434407.1:p.Val334=
ENST00000533005.5:n.763G>T
NM_006019.3:c.1650G>T	NP_006010.2:p.Val550=
NM_006053.3:c.1002G>T	NP_006044.1:p.Val334=
XM_005273709.2:c.1650G>T	XP_005273766.1:p.Val550=
XM_011544726.1:c.1650G>T	XP_011543028.1:p.Val550=
XM_011544727.1:c.1650G>T	XP_011543029.1:p.Val550=
XM_011544728.1:c.1650G>T	XP_011543030.1:p.Val550=
XR_949754.1:n.1654G>T
NM_001351059.1:c.756G>T	NP_001337988.1:p.Val252=
XM_024448320.1:c.1743G>T	XP_024304088.1:p.Val581=
XM_024448321.1:c.1743G>T	XP_024304089.1:p.Val581=
XM_024448322.1:c.1743G>T	XP_024304090.1:p.Val581=
XM_024448323.1:c.1743G>T	XP_024304091.1:p.Val581=
XM_024448324.1:c.1743G>T	XP_024304092.1:p.Val581=
XR_001747721.2:n.1774G>T
XR_001747722.1:n.1787G>T
XR_001747723.2:n.1787G>T
XR_002957115.1:n.1865G>T
NM_006019.4:c.1650G>T MANE Select	NP_006010.2:p.Val550=
NM_001351059.2:c.756G>T	NP_001337988.1:p.Val252=
NM_006053.4:c.1002G>T	NP_006044.1:p.Val334=