Canonical Allele Identifier: CA381584621
Gene: TCIRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047952T>C , CM000673.2:g.68047952T>C GRCh38
NC_000011.9:g.67815419T>C , CM000673.1:g.67815419T>C GRCh37
NC_000011.8:g.67571995T>C NCBI36
NG_007878.1:g.13937T>C , LRG_115:g.13937T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.159T>C
ENST00000698254.1:c.1063T>C ENSP00000513629.1:p.Tyr355His
ENST00000698255.1:c.1483T>C ENSP00000513630.1:p.Tyr495His
ENST00000698256.1:c.1000T>C
ENST00000698257.1:n.952T>C
ENST00000698258.1:n.669T>C
ENST00000698259.1:n.435T>C
ENST00000265686.8:c.1534T>C MANE Select ENSP00000265686.3:p.Tyr512His
ENST00000265686.7:c.1534T>C ENSP00000265686.3:p.Tyr512His
ENST00000525516.1:n.328T>C
ENST00000525724.5:n.846T>C
ENST00000528981.5:c.686T>C
ENST00000532635.5:c.886T>C ENSP00000434407.1:p.Tyr296His
ENST00000533005.5:n.647T>C
NM_006019.3:c.1534T>C NP_006010.2:p.Tyr512His
NM_006053.3:c.886T>C NP_006044.1:p.Tyr296His
XM_005273709.2:c.1534T>C XP_005273766.1:p.Tyr512His
XM_011544726.1:c.1534T>C XP_011543028.1:p.Tyr512His
XM_011544727.1:c.1534T>C XP_011543029.1:p.Tyr512His
XM_011544728.1:c.1534T>C XP_011543030.1:p.Tyr512His
XR_949754.1:n.1538T>C
NM_001351059.1:c.640T>C NP_001337988.1:p.Tyr214His
XM_024448320.1:c.1627T>C XP_024304088.1:p.Tyr543His
XM_024448321.1:c.1627T>C XP_024304089.1:p.Tyr543His
XM_024448322.1:c.1627T>C XP_024304090.1:p.Tyr543His
XM_024448323.1:c.1627T>C XP_024304091.1:p.Tyr543His
XM_024448324.1:c.1627T>C XP_024304092.1:p.Tyr543His
XR_001747721.2:n.1658T>C
XR_001747722.1:n.1671T>C
XR_001747723.2:n.1671T>C
XR_002957115.1:n.1749T>C
NM_006019.4:c.1534T>C MANE Select NP_006010.2:p.Tyr512His
NM_001351059.2:c.640T>C NP_001337988.1:p.Tyr214His
NM_006053.4:c.886T>C NP_006044.1:p.Tyr296His