Canonical Allele Identifier: CA381584568

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815394C>G (hg19) ; chr11:g.68047927C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047927C>G , CM000673.2:g.68047927C>G	GRCh38
NC_000011.9:g.67815394C>G , CM000673.1:g.67815394C>G	GRCh37
NC_000011.8:g.67571970C>G	NCBI36
NG_007878.1:g.13912C>G , LRG_115:g.13912C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.134C>G
ENST00000698254.1:c.1038C>G	ENSP00000513629.1:p.Asn346Lys
ENST00000698255.1:c.1458C>G	ENSP00000513630.1:p.Asn486Lys
ENST00000698256.1:c.975C>G
ENST00000698257.1:n.927C>G
ENST00000698258.1:n.644C>G
ENST00000698259.1:n.410C>G
ENST00000265686.8:c.1509C>G MANE Select	ENSP00000265686.3:p.Asn503Lys
ENST00000265686.7:c.1509C>G	ENSP00000265686.3:p.Asn503Lys
ENST00000525516.1:n.303C>G
ENST00000525724.5:n.821C>G
ENST00000528981.5:c.661C>G
ENST00000532635.5:c.861C>G	ENSP00000434407.1:p.Asn287Lys
ENST00000533005.5:n.622C>G
NM_006019.3:c.1509C>G	NP_006010.2:p.Asn503Lys
NM_006053.3:c.861C>G	NP_006044.1:p.Asn287Lys
XM_005273709.2:c.1509C>G	XP_005273766.1:p.Asn503Lys
XM_011544726.1:c.1509C>G	XP_011543028.1:p.Asn503Lys
XM_011544727.1:c.1509C>G	XP_011543029.1:p.Asn503Lys
XM_011544728.1:c.1509C>G	XP_011543030.1:p.Asn503Lys
XR_949754.1:n.1513C>G
NM_001351059.1:c.615C>G	NP_001337988.1:p.Asn205Lys
XM_024448320.1:c.1602C>G	XP_024304088.1:p.Asn534Lys
XM_024448321.1:c.1602C>G	XP_024304089.1:p.Asn534Lys
XM_024448322.1:c.1602C>G	XP_024304090.1:p.Asn534Lys
XM_024448323.1:c.1602C>G	XP_024304091.1:p.Asn534Lys
XM_024448324.1:c.1602C>G	XP_024304092.1:p.Asn534Lys
XR_001747721.2:n.1633C>G
XR_001747722.1:n.1646C>G
XR_001747723.2:n.1646C>G
XR_002957115.1:n.1724C>G
NM_006019.4:c.1509C>G MANE Select	NP_006010.2:p.Asn503Lys
NM_001351059.2:c.615C>G	NP_001337988.1:p.Asn205Lys
NM_006053.4:c.861C>G	NP_006044.1:p.Asn287Lys