Canonical Allele Identifier: CA381585284

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67816415G>C (hg19) ; chr11:g.68048948G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048948G>C , CM000673.2:g.68048948G>C	GRCh38
NC_000011.9:g.67816415G>C , CM000673.1:g.67816415G>C	GRCh37
NC_000011.8:g.67572991G>C	NCBI36
NG_007878.1:g.14933G>C , LRG_115:g.14933G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.249G>C
ENST00000698254.1:c.1153G>C	ENSP00000513629.1:p.Gly385Arg
ENST00000698255.1:c.1573G>C	ENSP00000513630.1:p.Gly525Arg
ENST00000698256.1:c.1090G>C
ENST00000698257.1:n.1042G>C
ENST00000698258.1:n.759G>C
ENST00000698259.1:n.525G>C
ENST00000265686.8:c.1624G>C MANE Select	ENSP00000265686.3:p.Gly542Arg
ENST00000265686.7:c.1624G>C	ENSP00000265686.3:p.Gly542Arg
ENST00000525724.5:n.936G>C
ENST00000532635.5:c.976G>C	ENSP00000434407.1:p.Gly326Arg
ENST00000533005.5:n.737G>C
NM_006019.3:c.1624G>C	NP_006010.2:p.Gly542Arg
NM_006053.3:c.976G>C	NP_006044.1:p.Gly326Arg
XM_005273709.2:c.1624G>C	XP_005273766.1:p.Gly542Arg
XM_011544726.1:c.1624G>C	XP_011543028.1:p.Gly542Arg
XM_011544727.1:c.1624G>C	XP_011543029.1:p.Gly542Arg
XM_011544728.1:c.1624G>C	XP_011543030.1:p.Gly542Arg
XR_949754.1:n.1628G>C
NM_001351059.1:c.730G>C	NP_001337988.1:p.Gly244Arg
XM_024448320.1:c.1717G>C	XP_024304088.1:p.Gly573Arg
XM_024448321.1:c.1717G>C	XP_024304089.1:p.Gly573Arg
XM_024448322.1:c.1717G>C	XP_024304090.1:p.Gly573Arg
XM_024448323.1:c.1717G>C	XP_024304091.1:p.Gly573Arg
XM_024448324.1:c.1717G>C	XP_024304092.1:p.Gly573Arg
XR_001747721.2:n.1748G>C
XR_001747722.1:n.1761G>C
XR_001747723.2:n.1761G>C
XR_002957115.1:n.1839G>C
NM_006019.4:c.1624G>C MANE Select	NP_006010.2:p.Gly542Arg
NM_001351059.2:c.730G>C	NP_001337988.1:p.Gly244Arg
NM_006053.4:c.976G>C	NP_006044.1:p.Gly326Arg