Canonical Allele Identifier: CA475513866

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047673-C-A
• MyVariant Identifiers: chr11:g.67815140C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047673C>A , CM000673.2:g.68047673C>A	GRCh38
NC_000011.9:g.67815140C>A , CM000673.1:g.67815140C>A	GRCh37
NC_000011.8:g.67571716C>A	NCBI36
NG_007878.1:g.13658C>A , LRG_115:g.13658C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.861C>A	ENSP00000513629.1:p.Arg287=
ENST00000698255.1:c.1281C>A	ENSP00000513630.1:p.Arg427=
ENST00000698256.1:c.798C>A
ENST00000698257.1:n.750C>A
ENST00000698258.1:n.390C>A
ENST00000698259.1:n.156C>A
ENST00000265686.8:c.1332C>A MANE Select	ENSP00000265686.3:p.Arg444=
ENST00000265686.7:c.1332C>A	ENSP00000265686.3:p.Arg444=
ENST00000525516.1:n.126C>A
ENST00000525724.5:n.644C>A
ENST00000528981.5:c.484C>A
ENST00000529364.1:c.743C>A
ENST00000532635.5:c.684C>A	ENSP00000434407.1:p.Arg228=
ENST00000533005.5:n.368C>A
NM_006019.3:c.1332C>A	NP_006010.2:p.Arg444=
NM_006053.3:c.684C>A	NP_006044.1:p.Arg228=
XM_005273709.2:c.1332C>A	XP_005273766.1:p.Arg444=
XM_011544726.1:c.1332C>A	XP_011543028.1:p.Arg444=
XM_011544727.1:c.1332C>A	XP_011543029.1:p.Arg444=
XM_011544728.1:c.1332C>A	XP_011543030.1:p.Arg444=
XM_011544729.1:c.1348C>A	XP_011543031.1:p.Leu450Ile
XR_949754.1:n.1336C>A
NM_001351059.1:c.438C>A	NP_001337988.1:p.Arg146=
XM_024448320.1:c.1348C>A	XP_024304088.1:p.Leu450Ile
XM_024448321.1:c.1348C>A	XP_024304089.1:p.Leu450Ile
XM_024448322.1:c.1348C>A	XP_024304090.1:p.Leu450Ile
XM_024448323.1:c.1348C>A	XP_024304091.1:p.Leu450Ile
XM_024448324.1:c.1348C>A	XP_024304092.1:p.Leu450Ile
XR_001747721.2:n.1456C>A
XR_001747722.1:n.1469C>A
XR_001747723.2:n.1469C>A
XR_002957115.1:n.1470C>A
NM_006019.4:c.1332C>A MANE Select	NP_006010.2:p.Arg444=
NM_001351059.2:c.438C>A	NP_001337988.1:p.Arg146=
NM_006053.4:c.684C>A	NP_006044.1:p.Arg228=