Canonical Allele Identifier: CA6146870

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68044344G>A , CM000673.2:g.68044344G>A	GRCh38
NC_000011.9:g.67811811G>A , CM000673.1:g.67811811G>A	GRCh37
NC_000011.8:g.67568387G>A	NCBI36
NG_007878.1:g.10329G>A , LRG_115:g.10329G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.1020G>A MANE Select	NP_006010.2:p.Ser340=
ENST00000265686.8:c.1020G>A MANE Select	ENSP00000265686.3:p.Ser340=
NM_001351059.1:c.126G>A	NP_001337988.1:p.Ser42=
NM_001351059.2:c.126G>A	NP_001337988.1:p.Ser42=
NM_006019.3:c.1020G>A	NP_006010.2:p.Ser340=
NM_006053.3:c.372G>A	NP_006044.1:p.Ser124=
NM_006053.4:c.372G>A	NP_006044.1:p.Ser124=
ENST00000265686.7:c.1020G>A	ENSP00000265686.3:p.Ser340=
ENST00000525724.5:n.332G>A
ENST00000528981.5:c.110G>A
ENST00000529364.1:c.520G>A
ENST00000532635.5:c.372G>A	ENSP00000434407.1:p.Ser124=
ENST00000533005.5:n.56G>A
ENST00000698254.1:c.549G>A	ENSP00000513629.1:p.Ser183=
ENST00000698255.1:c.969G>A	ENSP00000513630.1:p.Ser323=
ENST00000698256.1:c.486G>A
ENST00000698257.1:n.438G>A
XM_005273709.2:c.1020G>A	XP_005273766.1:p.Ser340=
XM_011544726.1:c.1020G>A	XP_011543028.1:p.Ser340=
XM_011544727.1:c.1020G>A	XP_011543029.1:p.Ser340=
XM_011544728.1:c.1020G>A	XP_011543030.1:p.Ser340=
XM_011544729.1:c.1036G>A	XP_011543031.1:p.Asp346Asn
XM_024448320.1:c.1036G>A	XP_024304088.1:p.Asp346Asn
XM_024448321.1:c.1036G>A	XP_024304089.1:p.Asp346Asn
XM_024448322.1:c.1036G>A	XP_024304090.1:p.Asp346Asn
XM_024448323.1:c.1036G>A	XP_024304091.1:p.Asp346Asn
XM_024448324.1:c.1036G>A	XP_024304092.1:p.Asp346Asn
XR_001747721.2:n.1144G>A
XR_001747722.1:n.1157G>A
XR_001747723.2:n.1157G>A
XR_002957115.1:n.1158G>A
XR_949754.1:n.1024G>A