Canonical Allele Identifier: CA381583900

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815193A>T (hg19) ; chr11:g.68047726A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047726A>T , CM000673.2:g.68047726A>T	GRCh38
NC_000011.9:g.67815193A>T , CM000673.1:g.67815193A>T	GRCh37
NC_000011.8:g.67571769A>T	NCBI36
NG_007878.1:g.13711A>T , LRG_115:g.13711A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.10A>T
ENST00000698254.1:c.914A>T	ENSP00000513629.1:p.Asn305Ile
ENST00000698255.1:c.1334A>T	ENSP00000513630.1:p.Asn445Ile
ENST00000698256.1:c.851A>T
ENST00000698257.1:n.803A>T
ENST00000698258.1:n.443A>T
ENST00000698259.1:n.209A>T
ENST00000265686.8:c.1385A>T MANE Select	ENSP00000265686.3:p.Asn462Ile
ENST00000265686.7:c.1385A>T	ENSP00000265686.3:p.Asn462Ile
ENST00000525516.1:n.179A>T
ENST00000525724.5:n.697A>T
ENST00000528981.5:c.537A>T
ENST00000529364.1:c.796A>T
ENST00000532635.5:c.737A>T	ENSP00000434407.1:p.Asn246Ile
ENST00000533005.5:n.421A>T
NM_006019.3:c.1385A>T	NP_006010.2:p.Asn462Ile
NM_006053.3:c.737A>T	NP_006044.1:p.Asn246Ile
XM_005273709.2:c.1385A>T	XP_005273766.1:p.Asn462Ile
XM_011544726.1:c.1385A>T	XP_011543028.1:p.Asn462Ile
XM_011544727.1:c.1385A>T	XP_011543029.1:p.Asn462Ile
XM_011544728.1:c.1385A>T	XP_011543030.1:p.Asn462Ile
XM_011544729.1:c.1401A>T	XP_011543031.1:p.Gln467His
XR_949754.1:n.1389A>T
NM_001351059.1:c.491A>T	NP_001337988.1:p.Asn164Ile
XM_024448320.1:c.1401A>T	XP_024304088.1:p.Gln467His
XM_024448321.1:c.1401A>T	XP_024304089.1:p.Gln467His
XM_024448322.1:c.1401A>T	XP_024304090.1:p.Gln467His
XM_024448323.1:c.1401A>T	XP_024304091.1:p.Gln467His
XM_024448324.1:c.1401A>T	XP_024304092.1:p.Gln467His
XR_001747721.2:n.1509A>T
XR_001747722.1:n.1522A>T
XR_001747723.2:n.1522A>T
XR_002957115.1:n.1523A>T
NM_006019.4:c.1385A>T MANE Select	NP_006010.2:p.Asn462Ile
NM_001351059.2:c.491A>T	NP_001337988.1:p.Asn164Ile
NM_006053.4:c.737A>T	NP_006044.1:p.Asn246Ile