Canonical Allele Identifier: CA381584425

Gene: TCIRG1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.93G>T
ENST00000698254.1:c.997G>T	ENSP00000513629.1:p.Ala333Ser
ENST00000698255.1:c.1417G>T	ENSP00000513630.1:p.Ala473Ser
ENST00000698256.1:c.934G>T
ENST00000698257.1:n.886G>T
ENST00000698258.1:n.603G>T
ENST00000698259.1:n.369G>T
ENST00000265686.8:c.1468G>T MANE Select	ENSP00000265686.3:p.Ala490Ser
ENST00000265686.7:c.1468G>T	ENSP00000265686.3:p.Ala490Ser
ENST00000525516.1:n.262G>T
ENST00000525724.5:n.780G>T
ENST00000528981.5:c.620G>T
ENST00000532635.5:c.820G>T	ENSP00000434407.1:p.Ala274Ser
ENST00000533005.5:n.581G>T
NM_006019.3:c.1468G>T	NP_006010.2:p.Ala490Ser
NM_006053.3:c.820G>T	NP_006044.1:p.Ala274Ser
XM_005273709.2:c.1468G>T	XP_005273766.1:p.Ala490Ser
XM_011544726.1:c.1468G>T	XP_011543028.1:p.Ala490Ser
XM_011544727.1:c.1468G>T	XP_011543029.1:p.Ala490Ser
XM_011544728.1:c.1468G>T	XP_011543030.1:p.Ala490Ser
XM_011544729.1:c.*2G>T	XP_011543031.1:n.*2G>T
XR_949754.1:n.1472G>T
NM_001351059.1:c.574G>T	NP_001337988.1:p.Ala192Ser
XM_024448320.1:c.1561G>T	XP_024304088.1:p.Ala521Ser
XM_024448321.1:c.1561G>T	XP_024304089.1:p.Ala521Ser
XM_024448322.1:c.1561G>T	XP_024304090.1:p.Ala521Ser
XM_024448323.1:c.1561G>T	XP_024304091.1:p.Ala521Ser
XM_024448324.1:c.1561G>T	XP_024304092.1:p.Ala521Ser
XR_001747721.2:n.1592G>T
XR_001747722.1:n.1605G>T
XR_001747723.2:n.1605G>T
XR_002957115.1:n.1683G>T
NM_006019.4:c.1468G>T MANE Select	NP_006010.2:p.Ala490Ser
NM_001351059.2:c.574G>T	NP_001337988.1:p.Ala192Ser
NM_006053.4:c.820G>T	NP_006044.1:p.Ala274Ser