Canonical Allele Identifier: CA381584423

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815353G>A (hg19) ; chr11:g.68047886G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047886G>A , CM000673.2:g.68047886G>A	GRCh38
NC_000011.9:g.67815353G>A , CM000673.1:g.67815353G>A	GRCh37
NC_000011.8:g.67571929G>A	NCBI36
NG_007878.1:g.13871G>A , LRG_115:g.13871G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.93G>A
ENST00000698254.1:c.997G>A	ENSP00000513629.1:p.Ala333Thr
ENST00000698255.1:c.1417G>A	ENSP00000513630.1:p.Ala473Thr
ENST00000698256.1:c.934G>A
ENST00000698257.1:n.886G>A
ENST00000698258.1:n.603G>A
ENST00000698259.1:n.369G>A
ENST00000265686.8:c.1468G>A MANE Select	ENSP00000265686.3:p.Ala490Thr
ENST00000265686.7:c.1468G>A	ENSP00000265686.3:p.Ala490Thr
ENST00000525516.1:n.262G>A
ENST00000525724.5:n.780G>A
ENST00000528981.5:c.620G>A
ENST00000532635.5:c.820G>A	ENSP00000434407.1:p.Ala274Thr
ENST00000533005.5:n.581G>A
NM_006019.3:c.1468G>A	NP_006010.2:p.Ala490Thr
NM_006053.3:c.820G>A	NP_006044.1:p.Ala274Thr
XM_005273709.2:c.1468G>A	XP_005273766.1:p.Ala490Thr
XM_011544726.1:c.1468G>A	XP_011543028.1:p.Ala490Thr
XM_011544727.1:c.1468G>A	XP_011543029.1:p.Ala490Thr
XM_011544728.1:c.1468G>A	XP_011543030.1:p.Ala490Thr
XM_011544729.1:c.*2G>A	XP_011543031.1:n.*2G>A
XR_949754.1:n.1472G>A
NM_001351059.1:c.574G>A	NP_001337988.1:p.Ala192Thr
XM_024448320.1:c.1561G>A	XP_024304088.1:p.Ala521Thr
XM_024448321.1:c.1561G>A	XP_024304089.1:p.Ala521Thr
XM_024448322.1:c.1561G>A	XP_024304090.1:p.Ala521Thr
XM_024448323.1:c.1561G>A	XP_024304091.1:p.Ala521Thr
XM_024448324.1:c.1561G>A	XP_024304092.1:p.Ala521Thr
XR_001747721.2:n.1592G>A
XR_001747722.1:n.1605G>A
XR_001747723.2:n.1605G>A
XR_002957115.1:n.1683G>A
NM_006019.4:c.1468G>A MANE Select	NP_006010.2:p.Ala490Thr
NM_001351059.2:c.574G>A	NP_001337988.1:p.Ala192Thr
NM_006053.4:c.820G>A	NP_006044.1:p.Ala274Thr