Canonical Allele Identifier: CA475450246

Gene: TCIRG1

Linked Data

• dbSNP Id: rs1179623386
• gnomAD v2: 11-67816438-G-A
• gnomAD v4: 11-68048971-G-A
• MyVariant Identifiers: chr11:g.67816438G>A (hg19) ; chr11:g.68048971G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048971G>A , CM000673.2:g.68048971G>A	GRCh38
NC_000011.9:g.67816438G>A , CM000673.1:g.67816438G>A	GRCh37
NC_000011.8:g.67573014G>A	NCBI36
NG_007878.1:g.14956G>A , LRG_115:g.14956G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.272G>A
ENST00000698254.1:c.1176G>A	ENSP00000513629.1:p.Gly392=
ENST00000698255.1:c.1596G>A	ENSP00000513630.1:p.Gly532=
ENST00000698256.1:c.1113G>A
ENST00000698257.1:n.1065G>A
ENST00000698258.1:n.782G>A
ENST00000698259.1:n.548G>A
ENST00000265686.8:c.1647G>A MANE Select	ENSP00000265686.3:p.Gly549=
ENST00000265686.7:c.1647G>A	ENSP00000265686.3:p.Gly549=
ENST00000525724.5:n.959G>A
ENST00000532635.5:c.999G>A	ENSP00000434407.1:p.Gly333=
ENST00000533005.5:n.760G>A
NM_006019.3:c.1647G>A	NP_006010.2:p.Gly549=
NM_006053.3:c.999G>A	NP_006044.1:p.Gly333=
XM_005273709.2:c.1647G>A	XP_005273766.1:p.Gly549=
XM_011544726.1:c.1647G>A	XP_011543028.1:p.Gly549=
XM_011544727.1:c.1647G>A	XP_011543029.1:p.Gly549=
XM_011544728.1:c.1647G>A	XP_011543030.1:p.Gly549=
XR_949754.1:n.1651G>A
NM_001351059.1:c.753G>A	NP_001337988.1:p.Gly251=
XM_024448320.1:c.1740G>A	XP_024304088.1:p.Gly580=
XM_024448321.1:c.1740G>A	XP_024304089.1:p.Gly580=
XM_024448322.1:c.1740G>A	XP_024304090.1:p.Gly580=
XM_024448323.1:c.1740G>A	XP_024304091.1:p.Gly580=
XM_024448324.1:c.1740G>A	XP_024304092.1:p.Gly580=
XR_001747721.2:n.1771G>A
XR_001747722.1:n.1784G>A
XR_001747723.2:n.1784G>A
XR_002957115.1:n.1862G>A
NM_006019.4:c.1647G>A MANE Select	NP_006010.2:p.Gly549=
NM_001351059.2:c.753G>A	NP_001337988.1:p.Gly251=
NM_006053.4:c.999G>A	NP_006044.1:p.Gly333=