Canonical Allele Identifier: CA381584312

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815264G>C (hg19) ; chr11:g.68047797G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047797G>C , CM000673.2:g.68047797G>C	GRCh38
NC_000011.9:g.67815264G>C , CM000673.1:g.67815264G>C	GRCh37
NC_000011.8:g.67571840G>C	NCBI36
NG_007878.1:g.13782G>C , LRG_115:g.13782G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.81G>C
ENST00000698254.1:c.985G>C	ENSP00000513629.1:p.Gly329Arg
ENST00000698255.1:c.1405G>C	ENSP00000513630.1:p.Gly469Arg
ENST00000698256.1:c.922G>C
ENST00000698257.1:n.874G>C
ENST00000698258.1:n.514G>C
ENST00000698259.1:n.280G>C
ENST00000265686.8:c.1456G>C MANE Select	ENSP00000265686.3:p.Gly486Arg
ENST00000265686.7:c.1456G>C	ENSP00000265686.3:p.Gly486Arg
ENST00000525516.1:n.250G>C
ENST00000525724.5:n.768G>C
ENST00000528981.5:c.608G>C
ENST00000529364.1:c.867G>C
ENST00000532635.5:c.808G>C	ENSP00000434407.1:p.Gly270Arg
ENST00000533005.5:n.492G>C
NM_006019.3:c.1456G>C	NP_006010.2:p.Gly486Arg
NM_006053.3:c.808G>C	NP_006044.1:p.Gly270Arg
XM_005273709.2:c.1456G>C	XP_005273766.1:p.Gly486Arg
XM_011544726.1:c.1456G>C	XP_011543028.1:p.Gly486Arg
XM_011544727.1:c.1456G>C	XP_011543029.1:p.Gly486Arg
XM_011544728.1:c.1456G>C	XP_011543030.1:p.Gly486Arg
XM_011544729.1:c.1472G>C	XP_011543031.1:p.Trp491Ser
XR_949754.1:n.1460G>C
NM_001351059.1:c.562G>C	NP_001337988.1:p.Gly188Arg
XM_024448320.1:c.1472G>C	XP_024304088.1:p.Trp491Ser
XM_024448321.1:c.1472G>C	XP_024304089.1:p.Trp491Ser
XM_024448322.1:c.1472G>C	XP_024304090.1:p.Trp491Ser
XM_024448323.1:c.1472G>C	XP_024304091.1:p.Trp491Ser
XM_024448324.1:c.1472G>C	XP_024304092.1:p.Trp491Ser
XR_001747721.2:n.1580G>C
XR_001747722.1:n.1593G>C
XR_001747723.2:n.1593G>C
XR_002957115.1:n.1594G>C
NM_006019.4:c.1456G>C MANE Select	NP_006010.2:p.Gly486Arg
NM_001351059.2:c.562G>C	NP_001337988.1:p.Gly188Arg
NM_006053.4:c.808G>C	NP_006044.1:p.Gly270Arg