Canonical Allele Identifier: CA381584562

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815393A>C (hg19) ; chr11:g.68047926A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047926A>C , CM000673.2:g.68047926A>C	GRCh38
NC_000011.9:g.67815393A>C , CM000673.1:g.67815393A>C	GRCh37
NC_000011.8:g.67571969A>C	NCBI36
NG_007878.1:g.13911A>C , LRG_115:g.13911A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.133A>C
ENST00000698254.1:c.1037A>C	ENSP00000513629.1:p.Asn346Thr
ENST00000698255.1:c.1457A>C	ENSP00000513630.1:p.Asn486Thr
ENST00000698256.1:c.974A>C
ENST00000698257.1:n.926A>C
ENST00000698258.1:n.643A>C
ENST00000698259.1:n.409A>C
ENST00000265686.8:c.1508A>C MANE Select	ENSP00000265686.3:p.Asn503Thr
ENST00000265686.7:c.1508A>C	ENSP00000265686.3:p.Asn503Thr
ENST00000525516.1:n.302A>C
ENST00000525724.5:n.820A>C
ENST00000528981.5:c.660A>C
ENST00000532635.5:c.860A>C	ENSP00000434407.1:p.Asn287Thr
ENST00000533005.5:n.621A>C
NM_006019.3:c.1508A>C	NP_006010.2:p.Asn503Thr
NM_006053.3:c.860A>C	NP_006044.1:p.Asn287Thr
XM_005273709.2:c.1508A>C	XP_005273766.1:p.Asn503Thr
XM_011544726.1:c.1508A>C	XP_011543028.1:p.Asn503Thr
XM_011544727.1:c.1508A>C	XP_011543029.1:p.Asn503Thr
XM_011544728.1:c.1508A>C	XP_011543030.1:p.Asn503Thr
XR_949754.1:n.1512A>C
NM_001351059.1:c.614A>C	NP_001337988.1:p.Asn205Thr
XM_024448320.1:c.1601A>C	XP_024304088.1:p.Asn534Thr
XM_024448321.1:c.1601A>C	XP_024304089.1:p.Asn534Thr
XM_024448322.1:c.1601A>C	XP_024304090.1:p.Asn534Thr
XM_024448323.1:c.1601A>C	XP_024304091.1:p.Asn534Thr
XM_024448324.1:c.1601A>C	XP_024304092.1:p.Asn534Thr
XR_001747721.2:n.1632A>C
XR_001747722.1:n.1645A>C
XR_001747723.2:n.1645A>C
XR_002957115.1:n.1723A>C
NM_006019.4:c.1508A>C MANE Select	NP_006010.2:p.Asn503Thr
NM_001351059.2:c.614A>C	NP_001337988.1:p.Asn205Thr
NM_006053.4:c.860A>C	NP_006044.1:p.Asn287Thr