Canonical Allele Identifier: CA475513849

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815116C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047649C>T , CM000673.2:g.68047649C>T	GRCh38
NC_000011.9:g.67815116C>T , CM000673.1:g.67815116C>T	GRCh37
NC_000011.8:g.67571692C>T	NCBI36
NG_007878.1:g.13634C>T , LRG_115:g.13634C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.837C>T	ENSP00000513629.1:p.Ile279=
ENST00000698255.1:c.1257C>T	ENSP00000513630.1:p.Ile419=
ENST00000698256.1:c.774C>T
ENST00000698257.1:n.726C>T
ENST00000698258.1:n.366C>T
ENST00000698259.1:n.132C>T
ENST00000265686.8:c.1308C>T MANE Select	ENSP00000265686.3:p.Ile436=
ENST00000265686.7:c.1308C>T	ENSP00000265686.3:p.Ile436=
ENST00000525516.1:n.102C>T
ENST00000525724.5:n.620C>T
ENST00000528981.5:c.460C>T
ENST00000529364.1:c.719C>T
ENST00000532635.5:c.660C>T	ENSP00000434407.1:p.Ile220=
ENST00000533005.5:n.344C>T
NM_006019.3:c.1308C>T	NP_006010.2:p.Ile436=
NM_006053.3:c.660C>T	NP_006044.1:p.Ile220=
XM_005273709.2:c.1308C>T	XP_005273766.1:p.Ile436=
XM_011544726.1:c.1308C>T	XP_011543028.1:p.Ile436=
XM_011544727.1:c.1308C>T	XP_011543029.1:p.Ile436=
XM_011544728.1:c.1308C>T	XP_011543030.1:p.Ile436=
XM_011544729.1:c.1324C>T	XP_011543031.1:p.Leu442=
XR_949754.1:n.1312C>T
NM_001351059.1:c.414C>T	NP_001337988.1:p.Ile138=
XM_024448320.1:c.1324C>T	XP_024304088.1:p.Leu442=
XM_024448321.1:c.1324C>T	XP_024304089.1:p.Leu442=
XM_024448322.1:c.1324C>T	XP_024304090.1:p.Leu442=
XM_024448323.1:c.1324C>T	XP_024304091.1:p.Leu442=
XM_024448324.1:c.1324C>T	XP_024304092.1:p.Leu442=
XR_001747721.2:n.1432C>T
XR_001747722.1:n.1445C>T
XR_001747723.2:n.1445C>T
XR_002957115.1:n.1446C>T
NM_006019.4:c.1308C>T MANE Select	NP_006010.2:p.Ile436=
NM_001351059.2:c.414C>T	NP_001337988.1:p.Ile138=
NM_006053.4:c.660C>T	NP_006044.1:p.Ile220=