Canonical Allele Identifier: CA475449711

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047488-G-T
• MyVariant Identifiers: chr11:g.67814955G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047488G>T , CM000673.2:g.68047488G>T	GRCh38
NC_000011.9:g.67814955G>T , CM000673.1:g.67814955G>T	GRCh37
NC_000011.8:g.67571531G>T	NCBI36
NG_007878.1:g.13473G>T , LRG_115:g.13473G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.750G>T	ENSP00000513629.1:p.Val250=
ENST00000698255.1:c.1170G>T	ENSP00000513630.1:p.Val390=
ENST00000698256.1:c.687G>T
ENST00000698257.1:n.639G>T
ENST00000698258.1:n.205G>T
ENST00000698259.1:n.45G>T
ENST00000265686.8:c.1221G>T MANE Select	ENSP00000265686.3:p.Val407=
ENST00000265686.7:c.1221G>T	ENSP00000265686.3:p.Val407=
ENST00000525516.1:n.15G>T
ENST00000525724.5:n.533G>T
ENST00000528981.5:c.373G>T
ENST00000529364.1:c.632G>T
ENST00000532635.5:c.573G>T	ENSP00000434407.1:p.Val191=
ENST00000533005.5:n.257G>T
NM_006019.3:c.1221G>T	NP_006010.2:p.Val407=
NM_006053.3:c.573G>T	NP_006044.1:p.Val191=
XM_005273709.2:c.1221G>T	XP_005273766.1:p.Val407=
XM_011544726.1:c.1221G>T	XP_011543028.1:p.Val407=
XM_011544727.1:c.1221G>T	XP_011543029.1:p.Val407=
XM_011544728.1:c.1221G>T	XP_011543030.1:p.Val407=
XM_011544729.1:c.1237G>T	XP_011543031.1:p.Gly413Trp
XR_949754.1:n.1225G>T
NM_001351059.1:c.327G>T	NP_001337988.1:p.Val109=
XM_024448320.1:c.1237G>T	XP_024304088.1:p.Gly413Trp
XM_024448321.1:c.1237G>T	XP_024304089.1:p.Gly413Trp
XM_024448322.1:c.1237G>T	XP_024304090.1:p.Gly413Trp
XM_024448323.1:c.1237G>T	XP_024304091.1:p.Gly413Trp
XM_024448324.1:c.1237G>T	XP_024304092.1:p.Gly413Trp
XR_001747721.2:n.1345G>T
XR_001747722.1:n.1358G>T
XR_001747723.2:n.1358G>T
XR_002957115.1:n.1359G>T
NM_006019.4:c.1221G>T MANE Select	NP_006010.2:p.Val407=
NM_001351059.2:c.327G>T	NP_001337988.1:p.Val109=
NM_006053.4:c.573G>T	NP_006044.1:p.Val191=