Canonical Allele Identifier: CA381582248

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67814956G>C (hg19) ; chr11:g.68047489G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047489G>C , CM000673.2:g.68047489G>C	GRCh38
NC_000011.9:g.67814956G>C , CM000673.1:g.67814956G>C	GRCh37
NC_000011.8:g.67571532G>C	NCBI36
NG_007878.1:g.13474G>C , LRG_115:g.13474G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.751G>C	ENSP00000513629.1:p.Gly251Arg
ENST00000698255.1:c.1171G>C	ENSP00000513630.1:p.Gly391Arg
ENST00000698256.1:c.688G>C
ENST00000698257.1:n.640G>C
ENST00000698258.1:n.206G>C
ENST00000698259.1:n.46G>C
ENST00000265686.8:c.1222G>C MANE Select	ENSP00000265686.3:p.Gly408Arg
ENST00000265686.7:c.1222G>C	ENSP00000265686.3:p.Gly408Arg
ENST00000525516.1:n.16G>C
ENST00000525724.5:n.534G>C
ENST00000528981.5:c.374G>C
ENST00000529364.1:c.633G>C
ENST00000532635.5:c.574G>C	ENSP00000434407.1:p.Gly192Arg
ENST00000533005.5:n.258G>C
NM_006019.3:c.1222G>C	NP_006010.2:p.Gly408Arg
NM_006053.3:c.574G>C	NP_006044.1:p.Gly192Arg
XM_005273709.2:c.1222G>C	XP_005273766.1:p.Gly408Arg
XM_011544726.1:c.1222G>C	XP_011543028.1:p.Gly408Arg
XM_011544727.1:c.1222G>C	XP_011543029.1:p.Gly408Arg
XM_011544728.1:c.1222G>C	XP_011543030.1:p.Gly408Arg
XM_011544729.1:c.1238G>C	XP_011543031.1:p.Gly413Ala
XR_949754.1:n.1226G>C
NM_001351059.1:c.328G>C	NP_001337988.1:p.Gly110Arg
XM_024448320.1:c.1238G>C	XP_024304088.1:p.Gly413Ala
XM_024448321.1:c.1238G>C	XP_024304089.1:p.Gly413Ala
XM_024448322.1:c.1238G>C	XP_024304090.1:p.Gly413Ala
XM_024448323.1:c.1238G>C	XP_024304091.1:p.Gly413Ala
XM_024448324.1:c.1238G>C	XP_024304092.1:p.Gly413Ala
XR_001747721.2:n.1346G>C
XR_001747722.1:n.1359G>C
XR_001747723.2:n.1359G>C
XR_002957115.1:n.1360G>C
NM_006019.4:c.1222G>C MANE Select	NP_006010.2:p.Gly408Arg
NM_001351059.2:c.328G>C	NP_001337988.1:p.Gly110Arg
NM_006053.4:c.574G>C	NP_006044.1:p.Gly192Arg