Canonical Allele Identifier: CA6146944

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68045033C>T , CM000673.2:g.68045033C>T	GRCh38
NC_000011.9:g.67812500C>T , CM000673.1:g.67812500C>T	GRCh37
NC_000011.8:g.67569076C>T	NCBI36
NG_007878.1:g.11018C>T , LRG_115:g.11018C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.1096C>T MANE Select	NP_006010.2:p.Arg366Cys
ENST00000265686.8:c.1096C>T MANE Select	ENSP00000265686.3:p.Arg366Cys
NM_001351059.1:c.202C>T	NP_001337988.1:p.Arg68Cys
NM_001351059.2:c.202C>T	NP_001337988.1:p.Arg68Cys
NM_006019.3:c.1096C>T	NP_006010.2:p.Arg366Cys
NM_006053.3:c.448C>T	NP_006044.1:p.Arg150Cys
NM_006053.4:c.448C>T	NP_006044.1:p.Arg150Cys
ENST00000265686.7:c.1096C>T	ENSP00000265686.3:p.Arg366Cys
ENST00000525724.5:n.408C>T
ENST00000528981.5:c.186C>T
ENST00000529364.1:c.521-14C>T
ENST00000532635.5:c.448C>T	ENSP00000434407.1:p.Arg150Cys
ENST00000533005.5:n.132C>T
ENST00000698254.1:c.625C>T	ENSP00000513629.1:p.Arg209Cys
ENST00000698255.1:c.1045C>T	ENSP00000513630.1:p.Arg349Cys
ENST00000698256.1:c.562C>T
ENST00000698257.1:n.514C>T
XM_005273709.2:c.1096C>T	XP_005273766.1:p.Arg366Cys
XM_011544726.1:c.1096C>T	XP_011543028.1:p.Arg366Cys
XM_011544727.1:c.1096C>T	XP_011543029.1:p.Arg366Cys
XM_011544728.1:c.1096C>T	XP_011543030.1:p.Arg366Cys
XM_011544729.1:c.1112C>T	XP_011543031.1:p.Pro371Leu
XM_024448320.1:c.1112C>T	XP_024304088.1:p.Pro371Leu
XM_024448321.1:c.1112C>T	XP_024304089.1:p.Pro371Leu
XM_024448322.1:c.1112C>T	XP_024304090.1:p.Pro371Leu
XM_024448323.1:c.1112C>T	XP_024304091.1:p.Pro371Leu
XM_024448324.1:c.1112C>T	XP_024304092.1:p.Pro371Leu
XR_001747721.2:n.1220C>T
XR_001747722.1:n.1233C>T
XR_001747723.2:n.1233C>T
XR_002957115.1:n.1234C>T
XR_949754.1:n.1100C>T