Canonical Allele Identifier: CA475513898

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815361G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047894G>C , CM000673.2:g.68047894G>C	GRCh38
NC_000011.9:g.67815361G>C , CM000673.1:g.67815361G>C	GRCh37
NC_000011.8:g.67571937G>C	NCBI36
NG_007878.1:g.13879G>C , LRG_115:g.13879G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.101G>C
ENST00000698254.1:c.1005G>C	ENSP00000513629.1:p.Leu335=
ENST00000698255.1:c.1425G>C	ENSP00000513630.1:p.Leu475=
ENST00000698256.1:c.942G>C
ENST00000698257.1:n.894G>C
ENST00000698258.1:n.611G>C
ENST00000698259.1:n.377G>C
ENST00000265686.8:c.1476G>C MANE Select	ENSP00000265686.3:p.Leu492=
ENST00000265686.7:c.1476G>C	ENSP00000265686.3:p.Leu492=
ENST00000525516.1:n.270G>C
ENST00000525724.5:n.788G>C
ENST00000528981.5:c.628G>C
ENST00000532635.5:c.828G>C	ENSP00000434407.1:p.Leu276=
ENST00000533005.5:n.589G>C
NM_006019.3:c.1476G>C	NP_006010.2:p.Leu492=
NM_006053.3:c.828G>C	NP_006044.1:p.Leu276=
XM_005273709.2:c.1476G>C	XP_005273766.1:p.Leu492=
XM_011544726.1:c.1476G>C	XP_011543028.1:p.Leu492=
XM_011544727.1:c.1476G>C	XP_011543029.1:p.Leu492=
XM_011544728.1:c.1476G>C	XP_011543030.1:p.Leu492=
XM_011544729.1:c.*10G>C	XP_011543031.1:n.*10G>C
XR_949754.1:n.1480G>C
NM_001351059.1:c.582G>C	NP_001337988.1:p.Leu194=
XM_024448320.1:c.1569G>C	XP_024304088.1:p.Leu523=
XM_024448321.1:c.1569G>C	XP_024304089.1:p.Leu523=
XM_024448322.1:c.1569G>C	XP_024304090.1:p.Leu523=
XM_024448323.1:c.1569G>C	XP_024304091.1:p.Leu523=
XM_024448324.1:c.1569G>C	XP_024304092.1:p.Leu523=
XR_001747721.2:n.1600G>C
XR_001747722.1:n.1613G>C
XR_001747723.2:n.1613G>C
XR_002957115.1:n.1691G>C
NM_006019.4:c.1476G>C MANE Select	NP_006010.2:p.Leu492=
NM_001351059.2:c.582G>C	NP_001337988.1:p.Leu194=
NM_006053.4:c.828G>C	NP_006044.1:p.Leu276=