Canonical Allele Identifier: CA475513948

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815391C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047924C>G , CM000673.2:g.68047924C>G	GRCh38
NC_000011.9:g.67815391C>G , CM000673.1:g.67815391C>G	GRCh37
NC_000011.8:g.67571967C>G	NCBI36
NG_007878.1:g.13909C>G , LRG_115:g.13909C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.131C>G
ENST00000698254.1:c.1035C>G	ENSP00000513629.1:p.Pro345=
ENST00000698255.1:c.1455C>G	ENSP00000513630.1:p.Pro485=
ENST00000698256.1:c.972C>G
ENST00000698257.1:n.924C>G
ENST00000698258.1:n.641C>G
ENST00000698259.1:n.407C>G
ENST00000265686.8:c.1506C>G MANE Select	ENSP00000265686.3:p.Pro502=
ENST00000265686.7:c.1506C>G	ENSP00000265686.3:p.Pro502=
ENST00000525516.1:n.300C>G
ENST00000525724.5:n.818C>G
ENST00000528981.5:c.658C>G
ENST00000532635.5:c.858C>G	ENSP00000434407.1:p.Pro286=
ENST00000533005.5:n.619C>G
NM_006019.3:c.1506C>G	NP_006010.2:p.Pro502=
NM_006053.3:c.858C>G	NP_006044.1:p.Pro286=
XM_005273709.2:c.1506C>G	XP_005273766.1:p.Pro502=
XM_011544726.1:c.1506C>G	XP_011543028.1:p.Pro502=
XM_011544727.1:c.1506C>G	XP_011543029.1:p.Pro502=
XM_011544728.1:c.1506C>G	XP_011543030.1:p.Pro502=
XR_949754.1:n.1510C>G
NM_001351059.1:c.612C>G	NP_001337988.1:p.Pro204=
XM_024448320.1:c.1599C>G	XP_024304088.1:p.Pro533=
XM_024448321.1:c.1599C>G	XP_024304089.1:p.Pro533=
XM_024448322.1:c.1599C>G	XP_024304090.1:p.Pro533=
XM_024448323.1:c.1599C>G	XP_024304091.1:p.Pro533=
XM_024448324.1:c.1599C>G	XP_024304092.1:p.Pro533=
XR_001747721.2:n.1630C>G
XR_001747722.1:n.1643C>G
XR_001747723.2:n.1643C>G
XR_002957115.1:n.1721C>G
NM_006019.4:c.1506C>G MANE Select	NP_006010.2:p.Pro502=
NM_001351059.2:c.612C>G	NP_001337988.1:p.Pro204=
NM_006053.4:c.858C>G	NP_006044.1:p.Pro286=