Canonical Allele Identifier: CA381583767

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815165T>C (hg19) ; chr11:g.68047698T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047698T>C , CM000673.2:g.68047698T>C	GRCh38
NC_000011.9:g.67815165T>C , CM000673.1:g.67815165T>C	GRCh37
NC_000011.8:g.67571741T>C	NCBI36
NG_007878.1:g.13683T>C , LRG_115:g.13683T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.886T>C	ENSP00000513629.1:p.Phe296Leu
ENST00000698255.1:c.1306T>C	ENSP00000513630.1:p.Phe436Leu
ENST00000698256.1:c.823T>C
ENST00000698257.1:n.775T>C
ENST00000698258.1:n.415T>C
ENST00000698259.1:n.181T>C
ENST00000265686.8:c.1357T>C MANE Select	ENSP00000265686.3:p.Phe453Leu
ENST00000265686.7:c.1357T>C	ENSP00000265686.3:p.Phe453Leu
ENST00000525516.1:n.151T>C
ENST00000525724.5:n.669T>C
ENST00000528981.5:c.509T>C
ENST00000529364.1:c.768T>C
ENST00000532635.5:c.709T>C	ENSP00000434407.1:p.Phe237Leu
ENST00000533005.5:n.393T>C
NM_006019.3:c.1357T>C	NP_006010.2:p.Phe453Leu
NM_006053.3:c.709T>C	NP_006044.1:p.Phe237Leu
XM_005273709.2:c.1357T>C	XP_005273766.1:p.Phe453Leu
XM_011544726.1:c.1357T>C	XP_011543028.1:p.Phe453Leu
XM_011544727.1:c.1357T>C	XP_011543029.1:p.Phe453Leu
XM_011544728.1:c.1357T>C	XP_011543030.1:p.Phe453Leu
XM_011544729.1:c.1373T>C	XP_011543031.1:p.Val458Ala
XR_949754.1:n.1361T>C
NM_001351059.1:c.463T>C	NP_001337988.1:p.Phe155Leu
XM_024448320.1:c.1373T>C	XP_024304088.1:p.Val458Ala
XM_024448321.1:c.1373T>C	XP_024304089.1:p.Val458Ala
XM_024448322.1:c.1373T>C	XP_024304090.1:p.Val458Ala
XM_024448323.1:c.1373T>C	XP_024304091.1:p.Val458Ala
XM_024448324.1:c.1373T>C	XP_024304092.1:p.Val458Ala
XR_001747721.2:n.1481T>C
XR_001747722.1:n.1494T>C
XR_001747723.2:n.1494T>C
XR_002957115.1:n.1495T>C
NM_006019.4:c.1357T>C MANE Select	NP_006010.2:p.Phe453Leu
NM_001351059.2:c.463T>C	NP_001337988.1:p.Phe155Leu
NM_006053.4:c.709T>C	NP_006044.1:p.Phe237Leu