Canonical Allele Identifier: CA381584581

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815398A>C (hg19) ; chr11:g.68047931A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047931A>C , CM000673.2:g.68047931A>C	GRCh38
NC_000011.9:g.67815398A>C , CM000673.1:g.67815398A>C	GRCh37
NC_000011.8:g.67571974A>C	NCBI36
NG_007878.1:g.13916A>C , LRG_115:g.13916A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.138A>C
ENST00000698254.1:c.1042A>C	ENSP00000513629.1:p.Thr348Pro
ENST00000698255.1:c.1462A>C	ENSP00000513630.1:p.Thr488Pro
ENST00000698256.1:c.979A>C
ENST00000698257.1:n.931A>C
ENST00000698258.1:n.648A>C
ENST00000698259.1:n.414A>C
ENST00000265686.8:c.1513A>C MANE Select	ENSP00000265686.3:p.Thr505Pro
ENST00000265686.7:c.1513A>C	ENSP00000265686.3:p.Thr505Pro
ENST00000525516.1:n.307A>C
ENST00000525724.5:n.825A>C
ENST00000528981.5:c.665A>C
ENST00000532635.5:c.865A>C	ENSP00000434407.1:p.Thr289Pro
ENST00000533005.5:n.626A>C
NM_006019.3:c.1513A>C	NP_006010.2:p.Thr505Pro
NM_006053.3:c.865A>C	NP_006044.1:p.Thr289Pro
XM_005273709.2:c.1513A>C	XP_005273766.1:p.Thr505Pro
XM_011544726.1:c.1513A>C	XP_011543028.1:p.Thr505Pro
XM_011544727.1:c.1513A>C	XP_011543029.1:p.Thr505Pro
XM_011544728.1:c.1513A>C	XP_011543030.1:p.Thr505Pro
XR_949754.1:n.1517A>C
NM_001351059.1:c.619A>C	NP_001337988.1:p.Thr207Pro
XM_024448320.1:c.1606A>C	XP_024304088.1:p.Thr536Pro
XM_024448321.1:c.1606A>C	XP_024304089.1:p.Thr536Pro
XM_024448322.1:c.1606A>C	XP_024304090.1:p.Thr536Pro
XM_024448323.1:c.1606A>C	XP_024304091.1:p.Thr536Pro
XM_024448324.1:c.1606A>C	XP_024304092.1:p.Thr536Pro
XR_001747721.2:n.1637A>C
XR_001747722.1:n.1650A>C
XR_001747723.2:n.1650A>C
XR_002957115.1:n.1728A>C
NM_006019.4:c.1513A>C MANE Select	NP_006010.2:p.Thr505Pro
NM_001351059.2:c.619A>C	NP_001337988.1:p.Thr207Pro
NM_006053.4:c.865A>C	NP_006044.1:p.Thr289Pro