Canonical Allele Identifier: CA475513905

Gene: TCIRG1

Linked Data

• ClinVar Variation Id: 2837335
• ClinVar RCV Id: RCV003692501
• MyVariant Identifiers: chr11:g.67815364C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047897C>G , CM000673.2:g.68047897C>G	GRCh38
NC_000011.9:g.67815364C>G , CM000673.1:g.67815364C>G	GRCh37
NC_000011.8:g.67571940C>G	NCBI36
NG_007878.1:g.13882C>G , LRG_115:g.13882C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.104C>G
ENST00000698254.1:c.1008C>G	ENSP00000513629.1:p.Ala336=
ENST00000698255.1:c.1428C>G	ENSP00000513630.1:p.Ala476=
ENST00000698256.1:c.945C>G
ENST00000698257.1:n.897C>G
ENST00000698258.1:n.614C>G
ENST00000698259.1:n.380C>G
ENST00000265686.8:c.1479C>G MANE Select	ENSP00000265686.3:p.Ala493=
ENST00000265686.7:c.1479C>G	ENSP00000265686.3:p.Ala493=
ENST00000525516.1:n.273C>G
ENST00000525724.5:n.791C>G
ENST00000528981.5:c.631C>G
ENST00000532635.5:c.831C>G	ENSP00000434407.1:p.Ala277=
ENST00000533005.5:n.592C>G
NM_006019.3:c.1479C>G	NP_006010.2:p.Ala493=
NM_006053.3:c.831C>G	NP_006044.1:p.Ala277=
XM_005273709.2:c.1479C>G	XP_005273766.1:p.Ala493=
XM_011544726.1:c.1479C>G	XP_011543028.1:p.Ala493=
XM_011544727.1:c.1479C>G	XP_011543029.1:p.Ala493=
XM_011544728.1:c.1479C>G	XP_011543030.1:p.Ala493=
XR_949754.1:n.1483C>G
NM_001351059.1:c.585C>G	NP_001337988.1:p.Ala195=
XM_024448320.1:c.1572C>G	XP_024304088.1:p.Ala524=
XM_024448321.1:c.1572C>G	XP_024304089.1:p.Ala524=
XM_024448322.1:c.1572C>G	XP_024304090.1:p.Ala524=
XM_024448323.1:c.1572C>G	XP_024304091.1:p.Ala524=
XM_024448324.1:c.1572C>G	XP_024304092.1:p.Ala524=
XR_001747721.2:n.1603C>G
XR_001747722.1:n.1616C>G
XR_001747723.2:n.1616C>G
XR_002957115.1:n.1694C>G
NM_006019.4:c.1479C>G MANE Select	NP_006010.2:p.Ala493=
NM_001351059.2:c.585C>G	NP_001337988.1:p.Ala195=
NM_006053.4:c.831C>G	NP_006044.1:p.Ala277=