Canonical Allele Identifier: CA381583390

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815119G>A (hg19) ; chr11:g.68047652G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047652G>A , CM000673.2:g.68047652G>A	GRCh38
NC_000011.9:g.67815119G>A , CM000673.1:g.67815119G>A	GRCh37
NC_000011.8:g.67571695G>A	NCBI36
NG_007878.1:g.13637G>A , LRG_115:g.13637G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.840G>A	ENSP00000513629.1:p.Trp280Ter
ENST00000698255.1:c.1260G>A	ENSP00000513630.1:p.Trp420Ter
ENST00000698256.1:c.777G>A
ENST00000698257.1:n.729G>A
ENST00000698258.1:n.369G>A
ENST00000698259.1:n.135G>A
ENST00000265686.8:c.1311G>A MANE Select	ENSP00000265686.3:p.Trp437Ter
ENST00000265686.7:c.1311G>A	ENSP00000265686.3:p.Trp437Ter
ENST00000525516.1:n.105G>A
ENST00000525724.5:n.623G>A
ENST00000528981.5:c.463G>A
ENST00000529364.1:c.722G>A
ENST00000532635.5:c.663G>A	ENSP00000434407.1:p.Trp221Ter
ENST00000533005.5:n.347G>A
NM_006019.3:c.1311G>A	NP_006010.2:p.Trp437Ter
NM_006053.3:c.663G>A	NP_006044.1:p.Trp221Ter
XM_005273709.2:c.1311G>A	XP_005273766.1:p.Trp437Ter
XM_011544726.1:c.1311G>A	XP_011543028.1:p.Trp437Ter
XM_011544727.1:c.1311G>A	XP_011543029.1:p.Trp437Ter
XM_011544728.1:c.1311G>A	XP_011543030.1:p.Trp437Ter
XM_011544729.1:c.1327G>A	XP_011543031.1:p.Ala443Thr
XR_949754.1:n.1315G>A
NM_001351059.1:c.417G>A	NP_001337988.1:p.Trp139Ter
XM_024448320.1:c.1327G>A	XP_024304088.1:p.Ala443Thr
XM_024448321.1:c.1327G>A	XP_024304089.1:p.Ala443Thr
XM_024448322.1:c.1327G>A	XP_024304090.1:p.Ala443Thr
XM_024448323.1:c.1327G>A	XP_024304091.1:p.Ala443Thr
XM_024448324.1:c.1327G>A	XP_024304092.1:p.Ala443Thr
XR_001747721.2:n.1435G>A
XR_001747722.1:n.1448G>A
XR_001747723.2:n.1448G>A
XR_002957115.1:n.1449G>A
NM_006019.4:c.1311G>A MANE Select	NP_006010.2:p.Trp437Ter
NM_001351059.2:c.417G>A	NP_001337988.1:p.Trp139Ter
NM_006053.4:c.663G>A	NP_006044.1:p.Trp221Ter