Canonical Allele Identifier: CA475513885

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815355A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047888A>T , CM000673.2:g.68047888A>T	GRCh38
NC_000011.9:g.67815355A>T , CM000673.1:g.67815355A>T	GRCh37
NC_000011.8:g.67571931A>T	NCBI36
NG_007878.1:g.13873A>T , LRG_115:g.13873A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.95A>T
ENST00000698254.1:c.999A>T	ENSP00000513629.1:p.Ala333=
ENST00000698255.1:c.1419A>T	ENSP00000513630.1:p.Ala473=
ENST00000698256.1:c.936A>T
ENST00000698257.1:n.888A>T
ENST00000698258.1:n.605A>T
ENST00000698259.1:n.371A>T
ENST00000265686.8:c.1470A>T MANE Select	ENSP00000265686.3:p.Ala490=
ENST00000265686.7:c.1470A>T	ENSP00000265686.3:p.Ala490=
ENST00000525516.1:n.264A>T
ENST00000525724.5:n.782A>T
ENST00000528981.5:c.622A>T
ENST00000532635.5:c.822A>T	ENSP00000434407.1:p.Ala274=
ENST00000533005.5:n.583A>T
NM_006019.3:c.1470A>T	NP_006010.2:p.Ala490=
NM_006053.3:c.822A>T	NP_006044.1:p.Ala274=
XM_005273709.2:c.1470A>T	XP_005273766.1:p.Ala490=
XM_011544726.1:c.1470A>T	XP_011543028.1:p.Ala490=
XM_011544727.1:c.1470A>T	XP_011543029.1:p.Ala490=
XM_011544728.1:c.1470A>T	XP_011543030.1:p.Ala490=
XM_011544729.1:c.*4A>T	XP_011543031.1:n.*4A>T
XR_949754.1:n.1474A>T
NM_001351059.1:c.576A>T	NP_001337988.1:p.Ala192=
XM_024448320.1:c.1563A>T	XP_024304088.1:p.Ala521=
XM_024448321.1:c.1563A>T	XP_024304089.1:p.Ala521=
XM_024448322.1:c.1563A>T	XP_024304090.1:p.Ala521=
XM_024448323.1:c.1563A>T	XP_024304091.1:p.Ala521=
XM_024448324.1:c.1563A>T	XP_024304092.1:p.Ala521=
XR_001747721.2:n.1594A>T
XR_001747722.1:n.1607A>T
XR_001747723.2:n.1607A>T
XR_002957115.1:n.1685A>T
NM_006019.4:c.1470A>T MANE Select	NP_006010.2:p.Ala490=
NM_001351059.2:c.576A>T	NP_001337988.1:p.Ala192=
NM_006053.4:c.822A>T	NP_006044.1:p.Ala274=