Canonical Allele Identifier: CA1874111530
Community Standard Title: NM_002160.4(TNC):c.6022G= (p.Glu2008=)
Gene: TNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.115030304C= , CM000671.2:g.115030304C= GRCh38
NC_000009.11:g.117792583C= , CM000671.1:g.117792583C= GRCh37
NC_000009.10:g.116832404C= NCBI36
NG_029637.1:g.92954G=

Transcript Alleles

HGVS Amino-acid Change
NM_002160.4:c.6022G= MANE Select NP_002151.2:p.Glu2008=
ENST00000350763.9:c.6022G= MANE Select ENSP00000265131.4:p.Glu2008=
NM_002160.3:c.6022G= NP_002151.2:p.Glu2008=
ENST00000341037.8:c.5476G= ENSP00000339553.4:p.Glu1826=
ENST00000350763.8:c.6022G= ENSP00000265131.4:p.Glu2008=
ENST00000423613.6:c.5203G= ENSP00000411406.2:p.Glu1735=
ENST00000460345.1:n.604G=
ENST00000535648.5:c.4933G= ENSP00000438152.2:p.Glu1645=
ENST00000537320.5:c.4111G= ENSP00000443478.1:p.Glu1371=
ENST00000537320.6:c.4111G= ENSP00000443478.1:p.Glu1371=
ENST00000542877.5:c.4933G= ENSP00000442242.1:p.Glu1645=
ENST00000542877.6:c.4933G= ENSP00000442242.1:p.Glu1645=
ENST00000544972.1:c.1709G=
ENST00000705190.1:c.2965G= ENSP00000516083.1:p.Glu989=
ENST00000705191.1:c.1621G= ENSP00000516084.1:p.Glu541=
ENST00000705192.1:c.4980G=
XM_005251972.2:c.5749G= XP_005252029.1:p.Glu1917=
XM_005251972.4:c.5749G= XP_005252029.1:p.Glu1917=
XM_005251973.2:c.4930G= XP_005252030.1:p.Glu1644=
XM_005251973.4:c.4930G= XP_005252030.1:p.Glu1644=
XM_005251974.2:c.4384G= XP_005252031.1:p.Glu1462=
XM_005251974.4:c.4384G= XP_005252031.1:p.Glu1462=
XM_005251975.2:c.4111G= XP_005252032.1:p.Glu1371=
XM_005251975.4:c.4111G= XP_005252032.1:p.Glu1371=
XM_006717096.2:c.6298G= XP_006717159.1:p.Glu2100=
XM_006717096.4:c.6298G= XP_006717159.1:p.Glu2100=
XM_006717097.2:c.5749G= XP_006717160.1:p.Glu1917=
XM_006717097.4:c.5749G= XP_006717160.1:p.Glu1917=
XM_006717098.2:c.5476G= XP_006717161.1:p.Glu1826=
XM_006717098.4:c.5476G= XP_006717161.1:p.Glu1826=
XM_006717100.2:c.5203G= XP_006717163.1:p.Glu1735=
XM_006717101.2:c.4384G= XP_006717164.1:p.Glu1462=
XM_006717101.4:c.4384G= XP_006717164.1:p.Glu1462=
XM_011518622.1:c.6025G= XP_011516924.1:p.Glu2009=
XM_011518623.1:c.6025G= XP_011516925.1:p.Glu2009=
XM_011518624.1:c.5479G= XP_011516926.1:p.Glu1827=
XM_011518625.1:c.5476G= XP_011516927.1:p.Glu1826=
XM_011518625.3:c.5476G= XP_011516927.1:p.Glu1826=
XM_011518626.1:c.5206G= XP_011516928.1:p.Glu1736=
XM_011518626.3:c.5206G= XP_011516928.1:p.Glu1736=
XM_011518627.1:c.4933G= XP_011516929.1:p.Glu1645=
XM_011518628.1:c.4657G= XP_011516930.1:p.Glu1553=
XM_011518628.3:c.4657G= XP_011516930.1:p.Glu1553=
XM_011518629.1:c.4657G= XP_011516931.1:p.Glu1553=
XM_011518629.3:c.4657G= XP_011516931.1:p.Glu1553=
XM_017014678.2:c.6571G= XP_016870167.1:p.Glu2191=
XM_017014679.2:c.6298G= XP_016870168.1:p.Glu2100=
XM_017014680.2:c.6295G= XP_016870169.1:p.Glu2099=
XM_017014681.2:c.5479G= XP_016870170.1:p.Glu1827=
XM_024447530.1:c.6571G= XP_024303298.1:p.Glu2191=