Canonical Allele Identifier: CA475513881

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815146G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047679G>C , CM000673.2:g.68047679G>C	GRCh38
NC_000011.9:g.67815146G>C , CM000673.1:g.67815146G>C	GRCh37
NC_000011.8:g.67571722G>C	NCBI36
NG_007878.1:g.13664G>C , LRG_115:g.13664G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.867G>C	ENSP00000513629.1:p.Leu289=
ENST00000698255.1:c.1287G>C	ENSP00000513630.1:p.Leu429=
ENST00000698256.1:c.804G>C
ENST00000698257.1:n.756G>C
ENST00000698258.1:n.396G>C
ENST00000698259.1:n.162G>C
ENST00000265686.8:c.1338G>C MANE Select	ENSP00000265686.3:p.Leu446=
ENST00000265686.7:c.1338G>C	ENSP00000265686.3:p.Leu446=
ENST00000525516.1:n.132G>C
ENST00000525724.5:n.650G>C
ENST00000528981.5:c.490G>C
ENST00000529364.1:c.749G>C
ENST00000532635.5:c.690G>C	ENSP00000434407.1:p.Leu230=
ENST00000533005.5:n.374G>C
NM_006019.3:c.1338G>C	NP_006010.2:p.Leu446=
NM_006053.3:c.690G>C	NP_006044.1:p.Leu230=
XM_005273709.2:c.1338G>C	XP_005273766.1:p.Leu446=
XM_011544726.1:c.1338G>C	XP_011543028.1:p.Leu446=
XM_011544727.1:c.1338G>C	XP_011543029.1:p.Leu446=
XM_011544728.1:c.1338G>C	XP_011543030.1:p.Leu446=
XM_011544729.1:c.1354G>C	XP_011543031.1:p.Ala452Pro
XR_949754.1:n.1342G>C
NM_001351059.1:c.444G>C	NP_001337988.1:p.Leu148=
XM_024448320.1:c.1354G>C	XP_024304088.1:p.Ala452Pro
XM_024448321.1:c.1354G>C	XP_024304089.1:p.Ala452Pro
XM_024448322.1:c.1354G>C	XP_024304090.1:p.Ala452Pro
XM_024448323.1:c.1354G>C	XP_024304091.1:p.Ala452Pro
XM_024448324.1:c.1354G>C	XP_024304092.1:p.Ala452Pro
XR_001747721.2:n.1462G>C
XR_001747722.1:n.1475G>C
XR_001747723.2:n.1475G>C
XR_002957115.1:n.1476G>C
NM_006019.4:c.1338G>C MANE Select	NP_006010.2:p.Leu446=
NM_001351059.2:c.444G>C	NP_001337988.1:p.Leu148=
NM_006053.4:c.690G>C	NP_006044.1:p.Leu230=