Canonical Allele Identifier: CA6147442

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68050254C>T , CM000673.2:g.68050254C>T	GRCh38
NC_000011.9:g.67817721C>T , CM000673.1:g.67817721C>T	GRCh37
NC_000011.8:g.67574297C>T	NCBI36
NG_007878.1:g.16239C>T , LRG_115:g.16239C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.2236C>T MANE Select	NP_006010.2:p.Gln746Ter
ENST00000265686.8:c.2236C>T MANE Select	ENSP00000265686.3:p.Gln746Ter
NM_001351059.1:c.1342C>T	NP_001337988.1:p.Gln448Ter
NM_001351059.2:c.1342C>T	NP_001337988.1:p.Gln448Ter
NM_006019.3:c.2236C>T	NP_006010.2:p.Gln746Ter
NM_006053.3:c.1588C>T	NP_006044.1:p.Gln530Ter
NM_006053.4:c.1588C>T	NP_006044.1:p.Gln530Ter
ENST00000265686.7:c.2236C>T	ENSP00000265686.3:p.Gln746Ter
ENST00000525724.5:n.1548C>T
ENST00000530063.1:c.139C>T	ENSP00000432957.1:p.Arg47Trp
ENST00000530449.1:n.132C>T
ENST00000530449.2:n.1229C>T
ENST00000532635.5:c.1588C>T	ENSP00000434407.1:p.Gln530Ter
ENST00000533005.5:n.1349C>T
ENST00000698254.1:c.1765C>T	ENSP00000513629.1:p.Gln589Ter
ENST00000698255.1:c.2185C>T	ENSP00000513630.1:p.Gln729Ter
ENST00000698256.1:c.1702C>T
ENST00000698257.1:n.1654C>T
ENST00000698258.1:n.1371C>T
ENST00000698259.1:n.1505C>T
XM_005273709.2:c.2236C>T	XP_005273766.1:p.Gln746Ter
XM_011544726.1:c.2236C>T	XP_011543028.1:p.Gln746Ter
XM_011544727.1:c.2236C>T	XP_011543029.1:p.Arg746Trp
XM_024448320.1:c.2329C>T	XP_024304088.1:p.Gln777Ter
XM_024448321.1:c.2329C>T	XP_024304089.1:p.Gln777Ter
XM_024448322.1:c.2329C>T	XP_024304090.1:p.Gln777Ter
XM_024448323.1:c.2329C>T	XP_024304091.1:p.Gln777Ter
XR_001747721.2:n.2405C>T
XR_001747722.1:n.2373C>T
XR_001747723.2:n.2418C>T
XR_002957115.1:n.2594C>T
XR_949754.1:n.2383C>T