Canonical Allele Identifier: CA475514071

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815206T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047739T>C , CM000673.2:g.68047739T>C	GRCh38
NC_000011.9:g.67815206T>C , CM000673.1:g.67815206T>C	GRCh37
NC_000011.8:g.67571782T>C	NCBI36
NG_007878.1:g.13724T>C , LRG_115:g.13724T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.23T>C
ENST00000698254.1:c.927T>C	ENSP00000513629.1:p.Ser309=
ENST00000698255.1:c.1347T>C	ENSP00000513630.1:p.Ser449=
ENST00000698256.1:c.864T>C
ENST00000698257.1:n.816T>C
ENST00000698258.1:n.456T>C
ENST00000698259.1:n.222T>C
ENST00000265686.8:c.1398T>C MANE Select	ENSP00000265686.3:p.Ser466=
ENST00000265686.7:c.1398T>C	ENSP00000265686.3:p.Ser466=
ENST00000525516.1:n.192T>C
ENST00000525724.5:n.710T>C
ENST00000528981.5:c.550T>C
ENST00000529364.1:c.809T>C
ENST00000532635.5:c.750T>C	ENSP00000434407.1:p.Ser250=
ENST00000533005.5:n.434T>C
NM_006019.3:c.1398T>C	NP_006010.2:p.Ser466=
NM_006053.3:c.750T>C	NP_006044.1:p.Ser250=
XM_005273709.2:c.1398T>C	XP_005273766.1:p.Ser466=
XM_011544726.1:c.1398T>C	XP_011543028.1:p.Ser466=
XM_011544727.1:c.1398T>C	XP_011543029.1:p.Ser466=
XM_011544728.1:c.1398T>C	XP_011543030.1:p.Ser466=
XM_011544729.1:c.1414T>C	XP_011543031.1:p.Ser472Pro
XR_949754.1:n.1402T>C
NM_001351059.1:c.504T>C	NP_001337988.1:p.Ser168=
XM_024448320.1:c.1414T>C	XP_024304088.1:p.Ser472Pro
XM_024448321.1:c.1414T>C	XP_024304089.1:p.Ser472Pro
XM_024448322.1:c.1414T>C	XP_024304090.1:p.Ser472Pro
XM_024448323.1:c.1414T>C	XP_024304091.1:p.Ser472Pro
XM_024448324.1:c.1414T>C	XP_024304092.1:p.Ser472Pro
XR_001747721.2:n.1522T>C
XR_001747722.1:n.1535T>C
XR_001747723.2:n.1535T>C
XR_002957115.1:n.1536T>C
NM_006019.4:c.1398T>C MANE Select	NP_006010.2:p.Ser466=
NM_001351059.2:c.504T>C	NP_001337988.1:p.Ser168=
NM_006053.4:c.750T>C	NP_006044.1:p.Ser250=