Canonical Allele Identifier: CA381580963

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68044346T>A , CM000673.2:g.68044346T>A	GRCh38
NC_000011.9:g.67811813T>A , CM000673.1:g.67811813T>A	GRCh37
NC_000011.8:g.67568389T>A	NCBI36
NG_007878.1:g.10331T>A , LRG_115:g.10331T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.1020+2T>A MANE Select	NP_006010.2:n.1020+2T>A
ENST00000265686.8:c.1020+2T>A MANE Select	ENSP00000265686.3:n.1020+2T>A
NM_001351059.1:c.126+2T>A	NP_001337988.1:n.126+2T>A
NM_001351059.2:c.126+2T>A	NP_001337988.1:n.126+2T>A
NM_006019.3:c.1020+2T>A	NP_006010.2:n.1020+2T>A
NM_006053.3:c.372+2T>A	NP_006044.1:n.372+2T>A
NM_006053.4:c.372+2T>A	NP_006044.1:n.372+2T>A
ENST00000265686.7:c.1020+2T>A	ENSP00000265686.3:n.1020+2T>A
ENST00000525724.5:n.332+2T>A
ENST00000528981.5:c.110+2T>A
ENST00000529364.1:c.520+2T>A
ENST00000532635.5:c.372+2T>A	ENSP00000434407.1:n.372+2T>A
ENST00000533005.5:n.56+2T>A
ENST00000698254.1:c.549+2T>A	ENSP00000513629.1:n.549+2T>A
ENST00000698255.1:c.969+2T>A	ENSP00000513630.1:n.969+2T>A
ENST00000698256.1:c.486+2T>A
ENST00000698257.1:n.438+2T>A
XM_005273709.2:c.1020+2T>A	XP_005273766.1:n.1020+2T>A
XM_011544726.1:c.1020+2T>A	XP_011543028.1:n.1020+2T>A
XM_011544727.1:c.1020+2T>A	XP_011543029.1:n.1020+2T>A
XM_011544728.1:c.1020+2T>A	XP_011543030.1:n.1020+2T>A
XM_011544729.1:c.1036+2T>A	XP_011543031.1:n.1036+2T>A
XM_024448320.1:c.1036+2T>A	XP_024304088.1:n.1036+2T>A
XM_024448321.1:c.1036+2T>A	XP_024304089.1:n.1036+2T>A
XM_024448322.1:c.1036+2T>A	XP_024304090.1:n.1036+2T>A
XM_024448323.1:c.1036+2T>A	XP_024304091.1:n.1036+2T>A
XM_024448324.1:c.1036+2T>A	XP_024304092.1:n.1036+2T>A
XR_001747721.2:n.1144+2T>A
XR_001747722.1:n.1157+2T>A
XR_001747723.2:n.1157+2T>A
XR_002957115.1:n.1158+2T>A
XR_949754.1:n.1024+2T>A