Canonical Allele Identifier: CA5207442

Gene: TNC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115029385C>T , CM000671.2:g.115029385C>T	GRCh38
NC_000009.11:g.117791664C>T , CM000671.1:g.117791664C>T	GRCh37
NC_000009.10:g.116831485C>T	NCBI36
NG_029637.1:g.93873G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002160.4:c.6144G>A MANE Select	NP_002151.2:p.Gly2048=
ENST00000350763.9:c.6144G>A MANE Select	ENSP00000265131.4:p.Gly2048=
NM_002160.3:c.6144G>A	NP_002151.2:p.Gly2048=
ENST00000341037.8:c.5598G>A	ENSP00000339553.4:p.Gly1866=
ENST00000350763.8:c.6144G>A	ENSP00000265131.4:p.Gly2048=
ENST00000423613.6:c.5325G>A	ENSP00000411406.2:p.Gly1775=
ENST00000535648.5:c.5055G>A	ENSP00000438152.2:p.Gly1685=
ENST00000537320.5:c.4233G>A	ENSP00000443478.1:p.Gly1411=
ENST00000537320.6:c.4233G>A	ENSP00000443478.1:p.Gly1411=
ENST00000542877.5:c.5055G>A	ENSP00000442242.1:p.Gly1685=
ENST00000542877.6:c.5055G>A	ENSP00000442242.1:p.Gly1685=
ENST00000544972.1:c.1831G>A
ENST00000705190.1:c.3087G>A	ENSP00000516083.1:p.Gly1029=
ENST00000705191.1:c.1743G>A	ENSP00000516084.1:p.Gly581=
ENST00000705192.1:c.5102G>A
XM_005251972.2:c.5871G>A	XP_005252029.1:p.Gly1957=
XM_005251972.4:c.5871G>A	XP_005252029.1:p.Gly1957=
XM_005251973.2:c.5052G>A	XP_005252030.1:p.Gly1684=
XM_005251973.4:c.5052G>A	XP_005252030.1:p.Gly1684=
XM_005251974.2:c.4506G>A	XP_005252031.1:p.Gly1502=
XM_005251974.4:c.4506G>A	XP_005252031.1:p.Gly1502=
XM_005251975.2:c.4233G>A	XP_005252032.1:p.Gly1411=
XM_005251975.4:c.4233G>A	XP_005252032.1:p.Gly1411=
XM_006717096.2:c.6420G>A	XP_006717159.1:p.Gly2140=
XM_006717096.4:c.6420G>A	XP_006717159.1:p.Gly2140=
XM_006717097.2:c.5871G>A	XP_006717160.1:p.Gly1957=
XM_006717097.4:c.5871G>A	XP_006717160.1:p.Gly1957=
XM_006717098.2:c.5598G>A	XP_006717161.1:p.Gly1866=
XM_006717098.4:c.5598G>A	XP_006717161.1:p.Gly1866=
XM_006717100.2:c.5325G>A	XP_006717163.1:p.Gly1775=
XM_006717101.2:c.4506G>A	XP_006717164.1:p.Gly1502=
XM_006717101.4:c.4506G>A	XP_006717164.1:p.Gly1502=
XM_011518622.1:c.6147G>A	XP_011516924.1:p.Gly2049=
XM_011518623.1:c.6147G>A	XP_011516925.1:p.Gly2049=
XM_011518624.1:c.5601G>A	XP_011516926.1:p.Gly1867=
XM_011518625.1:c.5598G>A	XP_011516927.1:p.Gly1866=
XM_011518625.3:c.5598G>A	XP_011516927.1:p.Gly1866=
XM_011518626.1:c.5328G>A	XP_011516928.1:p.Gly1776=
XM_011518626.3:c.5328G>A	XP_011516928.1:p.Gly1776=
XM_011518627.1:c.5055G>A	XP_011516929.1:p.Gly1685=
XM_011518628.1:c.4779G>A	XP_011516930.1:p.Gly1593=
XM_011518628.3:c.4779G>A	XP_011516930.1:p.Gly1593=
XM_011518629.1:c.4779G>A	XP_011516931.1:p.Gly1593=
XM_011518629.3:c.4779G>A	XP_011516931.1:p.Gly1593=
XM_017014678.2:c.6693G>A	XP_016870167.1:p.Gly2231=
XM_017014679.2:c.6420G>A	XP_016870168.1:p.Gly2140=
XM_017014680.2:c.6417G>A	XP_016870169.1:p.Gly2139=
XM_017014681.2:c.5601G>A	XP_016870170.1:p.Gly1867=
XM_024447530.1:c.6693G>A	XP_024303298.1:p.Gly2231=