Canonical Allele Identifier: CA381584503

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815376G>C (hg19) ; chr11:g.68047909G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047909G>C , CM000673.2:g.68047909G>C	GRCh38
NC_000011.9:g.67815376G>C , CM000673.1:g.67815376G>C	GRCh37
NC_000011.8:g.67571952G>C	NCBI36
NG_007878.1:g.13894G>C , LRG_115:g.13894G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.116G>C
ENST00000698254.1:c.1020G>C	ENSP00000513629.1:p.Met340Ile
ENST00000698255.1:c.1440G>C	ENSP00000513630.1:p.Met480Ile
ENST00000698256.1:c.957G>C
ENST00000698257.1:n.909G>C
ENST00000698258.1:n.626G>C
ENST00000698259.1:n.392G>C
ENST00000265686.8:c.1491G>C MANE Select	ENSP00000265686.3:p.Met497Ile
ENST00000265686.7:c.1491G>C	ENSP00000265686.3:p.Met497Ile
ENST00000525516.1:n.285G>C
ENST00000525724.5:n.803G>C
ENST00000528981.5:c.643G>C
ENST00000532635.5:c.843G>C	ENSP00000434407.1:p.Met281Ile
ENST00000533005.5:n.604G>C
NM_006019.3:c.1491G>C	NP_006010.2:p.Met497Ile
NM_006053.3:c.843G>C	NP_006044.1:p.Met281Ile
XM_005273709.2:c.1491G>C	XP_005273766.1:p.Met497Ile
XM_011544726.1:c.1491G>C	XP_011543028.1:p.Met497Ile
XM_011544727.1:c.1491G>C	XP_011543029.1:p.Met497Ile
XM_011544728.1:c.1491G>C	XP_011543030.1:p.Met497Ile
XR_949754.1:n.1495G>C
NM_001351059.1:c.597G>C	NP_001337988.1:p.Met199Ile
XM_024448320.1:c.1584G>C	XP_024304088.1:p.Met528Ile
XM_024448321.1:c.1584G>C	XP_024304089.1:p.Met528Ile
XM_024448322.1:c.1584G>C	XP_024304090.1:p.Met528Ile
XM_024448323.1:c.1584G>C	XP_024304091.1:p.Met528Ile
XM_024448324.1:c.1584G>C	XP_024304092.1:p.Met528Ile
XR_001747721.2:n.1615G>C
XR_001747722.1:n.1628G>C
XR_001747723.2:n.1628G>C
XR_002957115.1:n.1706G>C
NM_006019.4:c.1491G>C MANE Select	NP_006010.2:p.Met497Ile
NM_001351059.2:c.597G>C	NP_001337988.1:p.Met199Ile
NM_006053.4:c.843G>C	NP_006044.1:p.Met281Ile