Canonical Allele Identifier: CA381582252

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67814957G>C (hg19) ; chr11:g.68047490G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047490G>C , CM000673.2:g.68047490G>C	GRCh38
NC_000011.9:g.67814957G>C , CM000673.1:g.67814957G>C	GRCh37
NC_000011.8:g.67571533G>C	NCBI36
NG_007878.1:g.13475G>C , LRG_115:g.13475G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.752G>C	ENSP00000513629.1:p.Gly251Ala
ENST00000698255.1:c.1172G>C	ENSP00000513630.1:p.Gly391Ala
ENST00000698256.1:c.689G>C
ENST00000698257.1:n.641G>C
ENST00000698258.1:n.207G>C
ENST00000698259.1:n.47G>C
ENST00000265686.8:c.1223G>C MANE Select	ENSP00000265686.3:p.Gly408Ala
ENST00000265686.7:c.1223G>C	ENSP00000265686.3:p.Gly408Ala
ENST00000525516.1:n.17G>C
ENST00000525724.5:n.535G>C
ENST00000528981.5:c.375G>C
ENST00000529364.1:c.634G>C
ENST00000532635.5:c.575G>C	ENSP00000434407.1:p.Gly192Ala
ENST00000533005.5:n.259G>C
NM_006019.3:c.1223G>C	NP_006010.2:p.Gly408Ala
NM_006053.3:c.575G>C	NP_006044.1:p.Gly192Ala
XM_005273709.2:c.1223G>C	XP_005273766.1:p.Gly408Ala
XM_011544726.1:c.1223G>C	XP_011543028.1:p.Gly408Ala
XM_011544727.1:c.1223G>C	XP_011543029.1:p.Gly408Ala
XM_011544728.1:c.1223G>C	XP_011543030.1:p.Gly408Ala
XM_011544729.1:c.1239G>C	XP_011543031.1:p.Gly413=
XR_949754.1:n.1227G>C
NM_001351059.1:c.329G>C	NP_001337988.1:p.Gly110Ala
XM_024448320.1:c.1239G>C	XP_024304088.1:p.Gly413=
XM_024448321.1:c.1239G>C	XP_024304089.1:p.Gly413=
XM_024448322.1:c.1239G>C	XP_024304090.1:p.Gly413=
XM_024448323.1:c.1239G>C	XP_024304091.1:p.Gly413=
XM_024448324.1:c.1239G>C	XP_024304092.1:p.Gly413=
XR_001747721.2:n.1347G>C
XR_001747722.1:n.1360G>C
XR_001747723.2:n.1360G>C
XR_002957115.1:n.1361G>C
NM_006019.4:c.1223G>C MANE Select	NP_006010.2:p.Gly408Ala
NM_001351059.2:c.329G>C	NP_001337988.1:p.Gly110Ala
NM_006053.4:c.575G>C	NP_006044.1:p.Gly192Ala