Canonical Allele Identifier: CA381580365

Gene: TCIRG1

Linked Data

• ClinVar Variation Id: 2679128
• ClinVar RCV Id: RCV003464680
• MyVariant Identifiers: chr11:g.67811689A>T (hg19) ; chr11:g.68044222A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68044222A>T , CM000673.2:g.68044222A>T	GRCh38
NC_000011.9:g.67811689A>T , CM000673.1:g.67811689A>T	GRCh37
NC_000011.8:g.67568265A>T	NCBI36
NG_007878.1:g.10207A>T , LRG_115:g.10207A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.427A>T	ENSP00000513629.1:p.Lys143Ter
ENST00000698255.1:c.847A>T	ENSP00000513630.1:p.Lys283Ter
ENST00000698256.1:c.364A>T
ENST00000698257.1:n.316A>T
ENST00000265686.8:c.898A>T MANE Select	ENSP00000265686.3:p.Lys300Ter
ENST00000265686.7:c.898A>T	ENSP00000265686.3:p.Lys300Ter
ENST00000524598.5:c.856A>T	ENSP00000432846.1:p.Lys286Ter
ENST00000525724.5:n.210A>T
ENST00000527530.1:n.516A>T
ENST00000529364.1:c.398A>T
ENST00000532635.5:c.250A>T	ENSP00000434407.1:p.Lys84Ter
NM_006019.3:c.898A>T	NP_006010.2:p.Lys300Ter
NM_006053.3:c.250A>T	NP_006044.1:p.Lys84Ter
XM_005273709.2:c.898A>T	XP_005273766.1:p.Lys300Ter
XM_011544726.1:c.898A>T	XP_011543028.1:p.Lys300Ter
XM_011544727.1:c.898A>T	XP_011543029.1:p.Lys300Ter
XM_011544728.1:c.898A>T	XP_011543030.1:p.Lys300Ter
XM_011544729.1:c.914A>T	XP_011543031.1:p.Glu305Val
XR_949754.1:n.902A>T
NM_001351059.1:c.4A>T	NP_001337988.1:p.Lys2Ter
XM_024448320.1:c.914A>T	XP_024304088.1:p.Glu305Val
XM_024448321.1:c.914A>T	XP_024304089.1:p.Glu305Val
XM_024448322.1:c.914A>T	XP_024304090.1:p.Glu305Val
XM_024448323.1:c.914A>T	XP_024304091.1:p.Glu305Val
XM_024448324.1:c.914A>T	XP_024304092.1:p.Glu305Val
XR_001747721.2:n.1022A>T
XR_001747722.1:n.1035A>T
XR_001747723.2:n.1035A>T
XR_002957115.1:n.1036A>T
NM_006019.4:c.898A>T MANE Select	NP_006010.2:p.Lys300Ter
NM_001351059.2:c.4A>T	NP_001337988.1:p.Lys2Ter
NM_006053.4:c.250A>T	NP_006044.1:p.Lys84Ter