Canonical Allele Identifier: CA381585091

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67816389T>C (hg19) ; chr11:g.68048922T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048922T>C , CM000673.2:g.68048922T>C	GRCh38
NC_000011.9:g.67816389T>C , CM000673.1:g.67816389T>C	GRCh37
NC_000011.8:g.67572965T>C	NCBI36
NG_007878.1:g.14907T>C , LRG_115:g.14907T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.223T>C
ENST00000698254.1:c.1127T>C	ENSP00000513629.1:p.Phe376Ser
ENST00000698255.1:c.1547T>C	ENSP00000513630.1:p.Phe516Ser
ENST00000698256.1:c.1064T>C
ENST00000698257.1:n.1016T>C
ENST00000698258.1:n.733T>C
ENST00000698259.1:n.499T>C
ENST00000265686.8:c.1598T>C MANE Select	ENSP00000265686.3:p.Phe533Ser
ENST00000265686.7:c.1598T>C	ENSP00000265686.3:p.Phe533Ser
ENST00000525724.5:n.910T>C
ENST00000528981.5:c.750T>C
ENST00000532635.5:c.950T>C	ENSP00000434407.1:p.Phe317Ser
ENST00000533005.5:n.711T>C
NM_006019.3:c.1598T>C	NP_006010.2:p.Phe533Ser
NM_006053.3:c.950T>C	NP_006044.1:p.Phe317Ser
XM_005273709.2:c.1598T>C	XP_005273766.1:p.Phe533Ser
XM_011544726.1:c.1598T>C	XP_011543028.1:p.Phe533Ser
XM_011544727.1:c.1598T>C	XP_011543029.1:p.Phe533Ser
XM_011544728.1:c.1598T>C	XP_011543030.1:p.Phe533Ser
XR_949754.1:n.1602T>C
NM_001351059.1:c.704T>C	NP_001337988.1:p.Phe235Ser
XM_024448320.1:c.1691T>C	XP_024304088.1:p.Phe564Ser
XM_024448321.1:c.1691T>C	XP_024304089.1:p.Phe564Ser
XM_024448322.1:c.1691T>C	XP_024304090.1:p.Phe564Ser
XM_024448323.1:c.1691T>C	XP_024304091.1:p.Phe564Ser
XM_024448324.1:c.1691T>C	XP_024304092.1:p.Phe564Ser
XR_001747721.2:n.1722T>C
XR_001747722.1:n.1735T>C
XR_001747723.2:n.1735T>C
XR_002957115.1:n.1813T>C
NM_006019.4:c.1598T>C MANE Select	NP_006010.2:p.Phe533Ser
NM_001351059.2:c.704T>C	NP_001337988.1:p.Phe235Ser
NM_006053.4:c.950T>C	NP_006044.1:p.Phe317Ser