Canonical Allele Identifier: CA381583434

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815123A>T (hg19) ; chr11:g.68047656A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047656A>T , CM000673.2:g.68047656A>T	GRCh38
NC_000011.9:g.67815123A>T , CM000673.1:g.67815123A>T	GRCh37
NC_000011.8:g.67571699A>T	NCBI36
NG_007878.1:g.13641A>T , LRG_115:g.13641A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.844A>T	ENSP00000513629.1:p.Thr282Ser
ENST00000698255.1:c.1264A>T	ENSP00000513630.1:p.Thr422Ser
ENST00000698256.1:c.781A>T
ENST00000698257.1:n.733A>T
ENST00000698258.1:n.373A>T
ENST00000698259.1:n.139A>T
ENST00000265686.8:c.1315A>T MANE Select	ENSP00000265686.3:p.Thr439Ser
ENST00000265686.7:c.1315A>T	ENSP00000265686.3:p.Thr439Ser
ENST00000525516.1:n.109A>T
ENST00000525724.5:n.627A>T
ENST00000528981.5:c.467A>T
ENST00000529364.1:c.726A>T
ENST00000532635.5:c.667A>T	ENSP00000434407.1:p.Thr223Ser
ENST00000533005.5:n.351A>T
NM_006019.3:c.1315A>T	NP_006010.2:p.Thr439Ser
NM_006053.3:c.667A>T	NP_006044.1:p.Thr223Ser
XM_005273709.2:c.1315A>T	XP_005273766.1:p.Thr439Ser
XM_011544726.1:c.1315A>T	XP_011543028.1:p.Thr439Ser
XM_011544727.1:c.1315A>T	XP_011543029.1:p.Thr439Ser
XM_011544728.1:c.1315A>T	XP_011543030.1:p.Thr439Ser
XM_011544729.1:c.1331A>T	XP_011543031.1:p.Asp444Val
XR_949754.1:n.1319A>T
NM_001351059.1:c.421A>T	NP_001337988.1:p.Thr141Ser
XM_024448320.1:c.1331A>T	XP_024304088.1:p.Asp444Val
XM_024448321.1:c.1331A>T	XP_024304089.1:p.Asp444Val
XM_024448322.1:c.1331A>T	XP_024304090.1:p.Asp444Val
XM_024448323.1:c.1331A>T	XP_024304091.1:p.Asp444Val
XM_024448324.1:c.1331A>T	XP_024304092.1:p.Asp444Val
XR_001747721.2:n.1439A>T
XR_001747722.1:n.1452A>T
XR_001747723.2:n.1452A>T
XR_002957115.1:n.1453A>T
NM_006019.4:c.1315A>T MANE Select	NP_006010.2:p.Thr439Ser
NM_001351059.2:c.421A>T	NP_001337988.1:p.Thr141Ser
NM_006053.4:c.667A>T	NP_006044.1:p.Thr223Ser