Canonical Allele Identifier: CA6146835

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68044150C>T , CM000673.2:g.68044150C>T	GRCh38
NC_000011.9:g.67811617C>T , CM000673.1:g.67811617C>T	GRCh37
NC_000011.8:g.67568193C>T	NCBI36
NG_007878.1:g.10135C>T , LRG_115:g.10135C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.826C>T MANE Select	NP_006010.2:p.Arg276Trp
ENST00000265686.8:c.826C>T MANE Select	ENSP00000265686.3:p.Arg276Trp
NM_001351059.1:c.-69C>T	NP_001337988.1:n.-69C>T
NM_001351059.2:c.-69C>T	NP_001337988.1:n.-69C>T
NM_006019.3:c.826C>T	NP_006010.2:p.Arg276Trp
NM_006053.3:c.178C>T	NP_006044.1:p.Arg60Trp
NM_006053.4:c.178C>T	NP_006044.1:p.Arg60Trp
ENST00000265686.7:c.826C>T	ENSP00000265686.3:p.Arg276Trp
ENST00000524598.5:c.784C>T	ENSP00000432846.1:p.Arg262Trp
ENST00000525724.5:n.138C>T
ENST00000527530.1:n.444C>T
ENST00000529364.1:c.326C>T
ENST00000532635.5:c.178C>T	ENSP00000434407.1:p.Arg60Trp
ENST00000534673.5:c.*174C>T	ENSP00000431174.1:n.*174C>T
ENST00000698254.1:c.404-49C>T	ENSP00000513629.1:n.404-49C>T
ENST00000698255.1:c.775C>T	ENSP00000513630.1:p.Arg259Trp
ENST00000698256.1:c.292C>T
ENST00000698257.1:n.244C>T
XM_005273709.2:c.826C>T	XP_005273766.1:p.Arg276Trp
XM_011544726.1:c.826C>T	XP_011543028.1:p.Arg276Trp
XM_011544727.1:c.826C>T	XP_011543029.1:p.Arg276Trp
XM_011544728.1:c.826C>T	XP_011543030.1:p.Arg276Trp
XM_011544729.1:c.842C>T	XP_011543031.1:p.Ala281Val
XM_024448320.1:c.842C>T	XP_024304088.1:p.Ala281Val
XM_024448321.1:c.842C>T	XP_024304089.1:p.Ala281Val
XM_024448322.1:c.842C>T	XP_024304090.1:p.Ala281Val
XM_024448323.1:c.842C>T	XP_024304091.1:p.Ala281Val
XM_024448324.1:c.842C>T	XP_024304092.1:p.Ala281Val
XR_001747721.2:n.950C>T
XR_001747722.1:n.963C>T
XR_001747723.2:n.963C>T
XR_002957115.1:n.964C>T
XR_949754.1:n.830C>T