Canonical Allele Identifier: CA381582425

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047543C>T , CM000673.2:g.68047543C>T	GRCh38
NC_000011.9:g.67815010C>T , CM000673.1:g.67815010C>T	GRCh37
NC_000011.8:g.67571586C>T	NCBI36
NG_007878.1:g.13528C>T , LRG_115:g.13528C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.1276C>T MANE Select	NP_006010.2:p.Arg426Ter
ENST00000265686.8:c.1276C>T MANE Select	ENSP00000265686.3:p.Arg426Ter
NM_001351059.1:c.382C>T	NP_001337988.1:p.Arg128Ter
NM_001351059.2:c.382C>T	NP_001337988.1:p.Arg128Ter
NM_006019.3:c.1276C>T	NP_006010.2:p.Arg426Ter
NM_006053.3:c.628C>T	NP_006044.1:p.Arg210Ter
NM_006053.4:c.628C>T	NP_006044.1:p.Arg210Ter
ENST00000265686.7:c.1276C>T	ENSP00000265686.3:p.Arg426Ter
ENST00000525516.1:n.70C>T
ENST00000525724.5:n.588C>T
ENST00000528981.5:c.428C>T
ENST00000529364.1:c.687C>T
ENST00000532635.5:c.628C>T	ENSP00000434407.1:p.Arg210Ter
ENST00000533005.5:n.312C>T
ENST00000698254.1:c.805C>T	ENSP00000513629.1:p.Arg269Ter
ENST00000698255.1:c.1225C>T	ENSP00000513630.1:p.Arg409Ter
ENST00000698256.1:c.742C>T
ENST00000698257.1:n.694C>T
ENST00000698258.1:n.260C>T
ENST00000698259.1:n.100C>T
XM_005273709.2:c.1276C>T	XP_005273766.1:p.Arg426Ter
XM_011544726.1:c.1276C>T	XP_011543028.1:p.Arg426Ter
XM_011544727.1:c.1276C>T	XP_011543029.1:p.Arg426Ter
XM_011544728.1:c.1276C>T	XP_011543030.1:p.Arg426Ter
XM_011544729.1:c.1292C>T	XP_011543031.1:p.Pro431Leu
XM_024448320.1:c.1292C>T	XP_024304088.1:p.Pro431Leu
XM_024448321.1:c.1292C>T	XP_024304089.1:p.Pro431Leu
XM_024448322.1:c.1292C>T	XP_024304090.1:p.Pro431Leu
XM_024448323.1:c.1292C>T	XP_024304091.1:p.Pro431Leu
XM_024448324.1:c.1292C>T	XP_024304092.1:p.Pro431Leu
XR_001747721.2:n.1400C>T
XR_001747722.1:n.1413C>T
XR_001747723.2:n.1413C>T
XR_002957115.1:n.1414C>T
XR_949754.1:n.1280C>T