Canonical Allele Identifier: CA381583335

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815113G>T (hg19) ; chr11:g.68047646G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047646G>T , CM000673.2:g.68047646G>T	GRCh38
NC_000011.9:g.67815113G>T , CM000673.1:g.67815113G>T	GRCh37
NC_000011.8:g.67571689G>T	NCBI36
NG_007878.1:g.13631G>T , LRG_115:g.13631G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.835-1G>T	ENSP00000513629.1:n.835-1G>T
ENST00000698255.1:c.1255-1G>T	ENSP00000513630.1:n.1255-1G>T
ENST00000698256.1:c.772-1G>T
ENST00000698257.1:n.724-1G>T
ENST00000698258.1:n.363G>T
ENST00000698259.1:n.130-1G>T
ENST00000265686.8:c.1306-1G>T MANE Select	ENSP00000265686.3:n.1306-1G>T
ENST00000265686.7:c.1306-1G>T	ENSP00000265686.3:n.1306-1G>T
ENST00000525516.1:n.100-1G>T
ENST00000525724.5:n.618-1G>T
ENST00000528981.5:c.458-1G>T
ENST00000529364.1:c.717-1G>T
ENST00000532635.5:c.658-1G>T	ENSP00000434407.1:n.658-1G>T
ENST00000533005.5:n.342-1G>T
NM_006019.3:c.1306-1G>T	NP_006010.2:n.1306-1G>T
NM_006053.3:c.658-1G>T	NP_006044.1:n.658-1G>T
XM_005273709.2:c.1306-1G>T	XP_005273766.1:n.1306-1G>T
XM_011544726.1:c.1306-1G>T	XP_011543028.1:n.1306-1G>T
XM_011544727.1:c.1306-1G>T	XP_011543029.1:n.1306-1G>T
XM_011544728.1:c.1306-1G>T	XP_011543030.1:n.1306-1G>T
XM_011544729.1:c.1322-1G>T	XP_011543031.1:n.1322-1G>T
XR_949754.1:n.1310-1G>T
NM_001351059.1:c.412-1G>T	NP_001337988.1:n.412-1G>T
XM_024448320.1:c.1322-1G>T	XP_024304088.1:n.1322-1G>T
XM_024448321.1:c.1322-1G>T	XP_024304089.1:n.1322-1G>T
XM_024448322.1:c.1322-1G>T	XP_024304090.1:n.1322-1G>T
XM_024448323.1:c.1322-1G>T	XP_024304091.1:n.1322-1G>T
XM_024448324.1:c.1322-1G>T	XP_024304092.1:n.1322-1G>T
XR_001747721.2:n.1430-1G>T
XR_001747722.1:n.1443-1G>T
XR_001747723.2:n.1443-1G>T
XR_002957115.1:n.1444-1G>T
NM_006019.4:c.1306-1G>T MANE Select	NP_006010.2:n.1306-1G>T
NM_001351059.2:c.412-1G>T	NP_001337988.1:n.412-1G>T
NM_006053.4:c.658-1G>T	NP_006044.1:n.658-1G>T