Canonical Allele Identifier: CA381584898

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67816356T>C (hg19) ; chr11:g.68048889T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048889T>C , CM000673.2:g.68048889T>C	GRCh38
NC_000011.9:g.67816356T>C , CM000673.1:g.67816356T>C	GRCh37
NC_000011.8:g.67572932T>C	NCBI36
NG_007878.1:g.14874T>C , LRG_115:g.14874T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.190T>C
ENST00000698254.1:c.1094T>C	ENSP00000513629.1:p.Leu365Pro
ENST00000698255.1:c.1514T>C	ENSP00000513630.1:p.Leu505Pro
ENST00000698256.1:c.1031T>C
ENST00000698257.1:n.983T>C
ENST00000698258.1:n.700T>C
ENST00000698259.1:n.466T>C
ENST00000265686.8:c.1565T>C MANE Select	ENSP00000265686.3:p.Leu522Pro
ENST00000265686.7:c.1565T>C	ENSP00000265686.3:p.Leu522Pro
ENST00000525724.5:n.877T>C
ENST00000528981.5:c.717T>C
ENST00000532635.5:c.917T>C	ENSP00000434407.1:p.Leu306Pro
ENST00000533005.5:n.678T>C
NM_006019.3:c.1565T>C	NP_006010.2:p.Leu522Pro
NM_006053.3:c.917T>C	NP_006044.1:p.Leu306Pro
XM_005273709.2:c.1565T>C	XP_005273766.1:p.Leu522Pro
XM_011544726.1:c.1565T>C	XP_011543028.1:p.Leu522Pro
XM_011544727.1:c.1565T>C	XP_011543029.1:p.Leu522Pro
XM_011544728.1:c.1565T>C	XP_011543030.1:p.Leu522Pro
XR_949754.1:n.1569T>C
NM_001351059.1:c.671T>C	NP_001337988.1:p.Leu224Pro
XM_024448320.1:c.1658T>C	XP_024304088.1:p.Leu553Pro
XM_024448321.1:c.1658T>C	XP_024304089.1:p.Leu553Pro
XM_024448322.1:c.1658T>C	XP_024304090.1:p.Leu553Pro
XM_024448323.1:c.1658T>C	XP_024304091.1:p.Leu553Pro
XM_024448324.1:c.1658T>C	XP_024304092.1:p.Leu553Pro
XR_001747721.2:n.1689T>C
XR_001747722.1:n.1702T>C
XR_001747723.2:n.1702T>C
XR_002957115.1:n.1780T>C
NM_006019.4:c.1565T>C MANE Select	NP_006010.2:p.Leu522Pro
NM_001351059.2:c.671T>C	NP_001337988.1:p.Leu224Pro
NM_006053.4:c.917T>C	NP_006044.1:p.Leu306Pro