Canonical Allele Identifier: CA6147088

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047713G>A , CM000673.2:g.68047713G>A	GRCh38
NC_000011.9:g.67815180G>A , CM000673.1:g.67815180G>A	GRCh37
NC_000011.8:g.67571756G>A	NCBI36
NG_007878.1:g.13698G>A , LRG_115:g.13698G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.1372G>A MANE Select	NP_006010.2:p.Gly458Ser
ENST00000265686.8:c.1372G>A MANE Select	ENSP00000265686.3:p.Gly458Ser
NM_001351059.1:c.478G>A	NP_001337988.1:p.Gly160Ser
NM_001351059.2:c.478G>A	NP_001337988.1:p.Gly160Ser
NM_006019.3:c.1372G>A	NP_006010.2:p.Gly458Ser
NM_006053.3:c.724G>A	NP_006044.1:p.Gly242Ser
NM_006053.4:c.724G>A	NP_006044.1:p.Gly242Ser
ENST00000265686.7:c.1372G>A	ENSP00000265686.3:p.Gly458Ser
ENST00000525516.1:n.166G>A
ENST00000525724.5:n.684G>A
ENST00000528981.5:c.524G>A
ENST00000529364.1:c.783G>A
ENST00000532635.5:c.724G>A	ENSP00000434407.1:p.Gly242Ser
ENST00000533005.5:n.408G>A
ENST00000698254.1:c.901G>A	ENSP00000513629.1:p.Gly301Ser
ENST00000698255.1:c.1321G>A	ENSP00000513630.1:p.Gly441Ser
ENST00000698256.1:c.838G>A
ENST00000698257.1:n.790G>A
ENST00000698258.1:n.430G>A
ENST00000698259.1:n.196G>A
XM_005273709.2:c.1372G>A	XP_005273766.1:p.Gly458Ser
XM_011544726.1:c.1372G>A	XP_011543028.1:p.Gly458Ser
XM_011544727.1:c.1372G>A	XP_011543029.1:p.Gly458Ser
XM_011544728.1:c.1372G>A	XP_011543030.1:p.Gly458Ser
XM_011544729.1:c.1388G>A	XP_011543031.1:p.Arg463Gln
XM_024448320.1:c.1388G>A	XP_024304088.1:p.Arg463Gln
XM_024448321.1:c.1388G>A	XP_024304089.1:p.Arg463Gln
XM_024448322.1:c.1388G>A	XP_024304090.1:p.Arg463Gln
XM_024448323.1:c.1388G>A	XP_024304091.1:p.Arg463Gln
XM_024448324.1:c.1388G>A	XP_024304092.1:p.Arg463Gln
XR_001747721.2:n.1496G>A
XR_001747722.1:n.1509G>A
XR_001747723.2:n.1509G>A
XR_002957115.1:n.1510G>A
XR_949754.1:n.1376G>A