Canonical Allele Identifier: CA381584648

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815428G>A (hg19) ; chr11:g.68047961G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047961G>A , CM000673.2:g.68047961G>A	GRCh38
NC_000011.9:g.67815428G>A , CM000673.1:g.67815428G>A	GRCh37
NC_000011.8:g.67572004G>A	NCBI36
NG_007878.1:g.13946G>A , LRG_115:g.13946G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.168G>A
ENST00000698254.1:c.1072G>A	ENSP00000513629.1:p.Gly358Ser
ENST00000698255.1:c.1492G>A	ENSP00000513630.1:p.Gly498Ser
ENST00000698256.1:c.1009G>A
ENST00000698257.1:n.961G>A
ENST00000698258.1:n.678G>A
ENST00000698259.1:n.444G>A
ENST00000265686.8:c.1543G>A MANE Select	ENSP00000265686.3:p.Gly515Ser
ENST00000265686.7:c.1543G>A	ENSP00000265686.3:p.Gly515Ser
ENST00000525516.1:n.337G>A
ENST00000525724.5:n.855G>A
ENST00000528981.5:c.695G>A
ENST00000532635.5:c.895G>A	ENSP00000434407.1:p.Gly299Ser
ENST00000533005.5:n.656G>A
NM_006019.3:c.1543G>A	NP_006010.2:p.Gly515Ser
NM_006053.3:c.895G>A	NP_006044.1:p.Gly299Ser
XM_005273709.2:c.1543G>A	XP_005273766.1:p.Gly515Ser
XM_011544726.1:c.1543G>A	XP_011543028.1:p.Gly515Ser
XM_011544727.1:c.1543G>A	XP_011543029.1:p.Gly515Ser
XM_011544728.1:c.1543G>A	XP_011543030.1:p.Gly515Ser
XR_949754.1:n.1547G>A
NM_001351059.1:c.649G>A	NP_001337988.1:p.Gly217Ser
XM_024448320.1:c.1636G>A	XP_024304088.1:p.Gly546Ser
XM_024448321.1:c.1636G>A	XP_024304089.1:p.Gly546Ser
XM_024448322.1:c.1636G>A	XP_024304090.1:p.Gly546Ser
XM_024448323.1:c.1636G>A	XP_024304091.1:p.Gly546Ser
XM_024448324.1:c.1636G>A	XP_024304092.1:p.Gly546Ser
XR_001747721.2:n.1667G>A
XR_001747722.1:n.1680G>A
XR_001747723.2:n.1680G>A
XR_002957115.1:n.1758G>A
NM_006019.4:c.1543G>A MANE Select	NP_006010.2:p.Gly515Ser
NM_001351059.2:c.649G>A	NP_001337988.1:p.Gly217Ser
NM_006053.4:c.895G>A	NP_006044.1:p.Gly299Ser