Canonical Allele Identifier: CA381585906

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68049091C>T , CM000673.2:g.68049091C>T	GRCh38
NC_000011.9:g.67816558C>T , CM000673.1:g.67816558C>T	GRCh37
NC_000011.8:g.67573134C>T	NCBI36
NG_007878.1:g.15076C>T , LRG_115:g.15076C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.1684C>T MANE Select	NP_006010.2:p.Gln562Ter
ENST00000265686.8:c.1684C>T MANE Select	ENSP00000265686.3:p.Gln562Ter
NM_001351059.1:c.790C>T	NP_001337988.1:p.Gln264Ter
NM_001351059.2:c.790C>T	NP_001337988.1:p.Gln264Ter
NM_006019.3:c.1684C>T	NP_006010.2:p.Gln562Ter
NM_006053.3:c.1036C>T	NP_006044.1:p.Gln346Ter
NM_006053.4:c.1036C>T	NP_006044.1:p.Gln346Ter
ENST00000265686.7:c.1684C>T	ENSP00000265686.3:p.Gln562Ter
ENST00000525724.5:n.996C>T
ENST00000530449.2:n.309C>T
ENST00000532635.5:c.1036C>T	ENSP00000434407.1:p.Gln346Ter
ENST00000533005.5:n.797C>T
ENST00000698254.1:c.1213C>T	ENSP00000513629.1:p.Gln405Ter
ENST00000698255.1:c.1633C>T	ENSP00000513630.1:p.Gln545Ter
ENST00000698256.1:c.1150C>T
ENST00000698257.1:n.1102C>T
ENST00000698258.1:n.819C>T
ENST00000698259.1:n.585C>T
XM_005273709.2:c.1684C>T	XP_005273766.1:p.Gln562Ter
XM_011544726.1:c.1684C>T	XP_011543028.1:p.Gln562Ter
XM_011544727.1:c.1684C>T	XP_011543029.1:p.Gln562Ter
XM_011544728.1:c.1684C>T	XP_011543030.1:p.Gln562Ter
XM_024448320.1:c.1777C>T	XP_024304088.1:p.Gln593Ter
XM_024448321.1:c.1777C>T	XP_024304089.1:p.Gln593Ter
XM_024448322.1:c.1777C>T	XP_024304090.1:p.Gln593Ter
XM_024448323.1:c.1777C>T	XP_024304091.1:p.Gln593Ter
XM_024448324.1:c.1777C>T	XP_024304092.1:p.Gln593Ter
XR_001747721.2:n.1808C>T
XR_001747722.1:n.1821C>T
XR_001747723.2:n.1821C>T
XR_002957115.1:n.1899C>T
XR_949754.1:n.1688C>T