Canonical Allele Identifier: CA198694637

Gene: TNC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115048730G>A , CM000671.2:g.115048730G>A	GRCh38
NC_000009.11:g.117811009G>A , CM000671.1:g.117811009G>A	GRCh37
NC_000009.10:g.116850830G>A	NCBI36
NG_029637.1:g.74528C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002160.4:c.4580-198C>T MANE Select	NP_002151.2:n.4580-198C>T
ENST00000350763.9:c.4580-198C>T MANE Select	ENSP00000265131.4:n.4580-198C>T
NM_002160.3:c.4580-198C>T	NP_002151.2:n.4580-198C>T
ENST00000341037.8:c.4307-2048C>T	ENSP00000339553.4:n.4307-2048C>T
ENST00000350763.8:c.4580-198C>T	ENSP00000265131.4:n.4580-198C>T
ENST00000423613.6:c.4307-6389C>T	ENSP00000411406.2:n.4307-6389C>T
ENST00000473855.1:n.171-2048C>T
ENST00000476680.1:n.253-6389C>T
ENST00000476680.2:c.318-6389C>T
ENST00000481475.1:n.551-198C>T
ENST00000498724.5:n.40-6389C>T
ENST00000535648.5:c.3764-2048C>T	ENSP00000438152.2:n.3764-2048C>T
ENST00000537320.5:c.3215-6389C>T	ENSP00000443478.1:n.3215-6389C>T
ENST00000537320.6:c.3215-6389C>T	ENSP00000443478.1:n.3215-6389C>T
ENST00000542877.5:c.3764-2048C>T	ENSP00000442242.1:n.3764-2048C>T
ENST00000542877.6:c.3764-2048C>T	ENSP00000442242.1:n.3764-2048C>T
ENST00000544972.1:c.540-2048C>T
ENST00000635336.1:c.11-2048C>T	ENSP00000489385.1:n.11-2048C>T
ENST00000705190.1:c.1523-198C>T	ENSP00000516083.1:n.1523-198C>T
ENST00000705191.1:c.179-198C>T	ENSP00000516084.1:n.179-198C>T
ENST00000705192.1:c.3811-2048C>T
XM_005251972.2:c.4580-2048C>T	XP_005252029.1:n.4580-2048C>T
XM_005251972.4:c.4580-2048C>T	XP_005252029.1:n.4580-2048C>T
XM_005251973.2:c.4034-6389C>T	XP_005252030.1:n.4034-6389C>T
XM_005251973.4:c.4034-6389C>T	XP_005252030.1:n.4034-6389C>T
XM_005251974.2:c.3215-2048C>T	XP_005252031.1:n.3215-2048C>T
XM_005251974.4:c.3215-2048C>T	XP_005252031.1:n.3215-2048C>T
XM_005251975.2:c.3215-6389C>T	XP_005252032.1:n.3215-6389C>T
XM_005251975.4:c.3215-6389C>T	XP_005252032.1:n.3215-6389C>T
XM_006717096.2:c.4856-198C>T	XP_006717159.1:n.4856-198C>T
XM_006717096.4:c.4856-198C>T	XP_006717159.1:n.4856-198C>T
XM_006717097.2:c.4307-198C>T	XP_006717160.1:n.4307-198C>T
XM_006717097.4:c.4307-198C>T	XP_006717160.1:n.4307-198C>T
XM_006717098.2:c.4307-2048C>T	XP_006717161.1:n.4307-2048C>T
XM_006717098.4:c.4307-2048C>T	XP_006717161.1:n.4307-2048C>T
XM_006717100.2:c.4307-6389C>T	XP_006717163.1:n.4307-6389C>T
XM_006717101.2:c.3488-6389C>T	XP_006717164.1:n.3488-6389C>T
XM_006717101.4:c.3488-6389C>T	XP_006717164.1:n.3488-6389C>T
XM_011518622.1:c.4856-2048C>T	XP_011516924.1:n.4856-2048C>T
XM_011518623.1:c.4583-198C>T	XP_011516925.1:n.4583-198C>T
XM_011518624.1:c.4037-198C>T	XP_011516926.1:n.4037-198C>T
XM_011518625.1:c.4580-6389C>T	XP_011516927.1:n.4580-6389C>T
XM_011518625.3:c.4580-6389C>T	XP_011516927.1:n.4580-6389C>T
XM_011518626.1:c.3764-198C>T	XP_011516928.1:n.3764-198C>T
XM_011518626.3:c.3764-198C>T	XP_011516928.1:n.3764-198C>T
XM_011518627.1:c.3764-2048C>T	XP_011516929.1:n.3764-2048C>T
XM_011518628.1:c.3761-6389C>T	XP_011516930.1:n.3761-6389C>T
XM_011518628.3:c.3761-6389C>T	XP_011516930.1:n.3761-6389C>T
XM_011518629.1:c.3488-2048C>T	XP_011516931.1:n.3488-2048C>T
XM_011518629.3:c.3488-2048C>T	XP_011516931.1:n.3488-2048C>T
XM_011518630.1:c.*264C>T	XP_011516932.1:n.*264C>T
XM_017014678.2:c.5129-198C>T	XP_016870167.1:n.5129-198C>T
XM_017014679.2:c.4856-198C>T	XP_016870168.1:n.4856-198C>T
XM_017014680.2:c.4853-198C>T	XP_016870169.1:n.4853-198C>T
XM_017014681.2:c.4037-198C>T	XP_016870170.1:n.4037-198C>T
XM_024447530.1:c.5129-198C>T	XP_024303298.1:n.5129-198C>T