Canonical Allele Identifier: CA475449715

Gene: TCIRG1

Linked Data

• ClinVar Variation Id: 2757496
• ClinVar RCV Id: RCV003567268
• MyVariant Identifiers: chr11:g.67814958C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047491C>A , CM000673.2:g.68047491C>A	GRCh38
NC_000011.9:g.67814958C>A , CM000673.1:g.67814958C>A	GRCh37
NC_000011.8:g.67571534C>A	NCBI36
NG_007878.1:g.13476C>A , LRG_115:g.13476C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698254.1:c.753C>A	ENSP00000513629.1:p.Gly251=
ENST00000698255.1:c.1173C>A	ENSP00000513630.1:p.Gly391=
ENST00000698256.1:c.690C>A
ENST00000698257.1:n.642C>A
ENST00000698258.1:n.208C>A
ENST00000698259.1:n.48C>A
ENST00000265686.8:c.1224C>A MANE Select	ENSP00000265686.3:p.Gly408=
ENST00000265686.7:c.1224C>A	ENSP00000265686.3:p.Gly408=
ENST00000525516.1:n.18C>A
ENST00000525724.5:n.536C>A
ENST00000528981.5:c.376C>A
ENST00000529364.1:c.635C>A
ENST00000532635.5:c.576C>A	ENSP00000434407.1:p.Gly192=
ENST00000533005.5:n.260C>A
NM_006019.3:c.1224C>A	NP_006010.2:p.Gly408=
NM_006053.3:c.576C>A	NP_006044.1:p.Gly192=
XM_005273709.2:c.1224C>A	XP_005273766.1:p.Gly408=
XM_011544726.1:c.1224C>A	XP_011543028.1:p.Gly408=
XM_011544727.1:c.1224C>A	XP_011543029.1:p.Gly408=
XM_011544728.1:c.1224C>A	XP_011543030.1:p.Gly408=
XM_011544729.1:c.1240C>A	XP_011543031.1:p.Pro414Thr
XR_949754.1:n.1228C>A
NM_001351059.1:c.330C>A	NP_001337988.1:p.Gly110=
XM_024448320.1:c.1240C>A	XP_024304088.1:p.Pro414Thr
XM_024448321.1:c.1240C>A	XP_024304089.1:p.Pro414Thr
XM_024448322.1:c.1240C>A	XP_024304090.1:p.Pro414Thr
XM_024448323.1:c.1240C>A	XP_024304091.1:p.Pro414Thr
XM_024448324.1:c.1240C>A	XP_024304092.1:p.Pro414Thr
XR_001747721.2:n.1348C>A
XR_001747722.1:n.1361C>A
XR_001747723.2:n.1361C>A
XR_002957115.1:n.1362C>A
NM_006019.4:c.1224C>A MANE Select	NP_006010.2:p.Gly408=
NM_001351059.2:c.330C>A	NP_001337988.1:p.Gly110=
NM_006053.4:c.576C>A	NP_006044.1:p.Gly192=