Canonical Allele Identifier: CA381584455

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815362G>C (hg19) ; chr11:g.68047895G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047895G>C , CM000673.2:g.68047895G>C	GRCh38
NC_000011.9:g.67815362G>C , CM000673.1:g.67815362G>C	GRCh37
NC_000011.8:g.67571938G>C	NCBI36
NG_007878.1:g.13880G>C , LRG_115:g.13880G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.102G>C
ENST00000698254.1:c.1006G>C	ENSP00000513629.1:p.Ala336Pro
ENST00000698255.1:c.1426G>C	ENSP00000513630.1:p.Ala476Pro
ENST00000698256.1:c.943G>C
ENST00000698257.1:n.895G>C
ENST00000698258.1:n.612G>C
ENST00000698259.1:n.378G>C
ENST00000265686.8:c.1477G>C MANE Select	ENSP00000265686.3:p.Ala493Pro
ENST00000265686.7:c.1477G>C	ENSP00000265686.3:p.Ala493Pro
ENST00000525516.1:n.271G>C
ENST00000525724.5:n.789G>C
ENST00000528981.5:c.629G>C
ENST00000532635.5:c.829G>C	ENSP00000434407.1:p.Ala277Pro
ENST00000533005.5:n.590G>C
NM_006019.3:c.1477G>C	NP_006010.2:p.Ala493Pro
NM_006053.3:c.829G>C	NP_006044.1:p.Ala277Pro
XM_005273709.2:c.1477G>C	XP_005273766.1:p.Ala493Pro
XM_011544726.1:c.1477G>C	XP_011543028.1:p.Ala493Pro
XM_011544727.1:c.1477G>C	XP_011543029.1:p.Ala493Pro
XM_011544728.1:c.1477G>C	XP_011543030.1:p.Ala493Pro
XM_011544729.1:c.*11G>C	XP_011543031.1:n.*11G>C
XR_949754.1:n.1481G>C
NM_001351059.1:c.583G>C	NP_001337988.1:p.Ala195Pro
XM_024448320.1:c.1570G>C	XP_024304088.1:p.Ala524Pro
XM_024448321.1:c.1570G>C	XP_024304089.1:p.Ala524Pro
XM_024448322.1:c.1570G>C	XP_024304090.1:p.Ala524Pro
XM_024448323.1:c.1570G>C	XP_024304091.1:p.Ala524Pro
XM_024448324.1:c.1570G>C	XP_024304092.1:p.Ala524Pro
XR_001747721.2:n.1601G>C
XR_001747722.1:n.1614G>C
XR_001747723.2:n.1614G>C
XR_002957115.1:n.1692G>C
NM_006019.4:c.1477G>C MANE Select	NP_006010.2:p.Ala493Pro
NM_001351059.2:c.583G>C	NP_001337988.1:p.Ala195Pro
NM_006053.4:c.829G>C	NP_006044.1:p.Ala277Pro