Canonical Allele Identifier: CA198692148

Gene: TNC

Linked Data

• dbSNP Id: rs1554796021
• gnomAD v2: 9-117808350-T-TTA
• gnomAD v3: 9-115046071-T-TTA
• gnomAD v4: 9-115046071-T-TTA
• MyVariant Identifiers: chr9:g.117808350_117808351insTA (hg19) ; chr9:g.117808351_117808352delinsTAAA (hg19) ; chr9:g.115046071_115046072insTA (hg38) ; chr9:g.115046072_115046073delinsTAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115046071_115046072insTA , CM000671.2:g.115046071_115046072insTA	GRCh38
NC_000009.11:g.117808350_117808351insTA , CM000671.1:g.117808350_117808351insTA	GRCh37
NC_000009.10:g.116848171_116848172insTA	NCBI36
NG_029637.1:g.77186_77187insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476680.2:c.318-3731_318-3730insTA
ENST00000537320.6:c.3215-3731_3215-3730insTA	ENSP00000443478.1:n.3215-3731_3215-3730insTA
ENST00000542877.6:c.4036+338_4036+339insTA	ENSP00000442242.1:n.4036+338_4036+339insTA
ENST00000705190.1:c.2068+338_2068+339insTA	ENSP00000516083.1:n.2068+338_2068+339insTA
ENST00000705191.1:c.724+338_724+339insTA	ENSP00000516084.1:n.724+338_724+339insTA
ENST00000705192.1:c.4083+338_4083+339insTA
ENST00000350763.9:c.5125+338_5125+339insTA MANE Select	ENSP00000265131.4:n.5125+338_5125+339insTA
ENST00000341037.8:c.4579+338_4579+339insTA	ENSP00000339553.4:n.4579+338_4579+339insTA
ENST00000350763.8:c.5125+338_5125+339insTA	ENSP00000265131.4:n.5125+338_5125+339insTA
ENST00000423613.6:c.4307-3731_4307-3730insTA	ENSP00000411406.2:n.4307-3731_4307-3730insTA
ENST00000476680.1:n.253-3731_253-3730insTA
ENST00000498724.5:n.40-3731_40-3730insTA
ENST00000535648.5:c.4036+338_4036+339insTA	ENSP00000438152.2:n.4036+338_4036+339insTA
ENST00000537320.5:c.3215-3731_3215-3730insTA	ENSP00000443478.1:n.3215-3731_3215-3730insTA
ENST00000542877.5:c.4036+338_4036+339insTA	ENSP00000442242.1:n.4036+338_4036+339insTA
ENST00000544972.1:c.812+338_812+339insTA
NM_002160.3:c.5125+338_5125+339insTA	NP_002151.2:n.5125+338_5125+339insTA
XM_005251972.2:c.4852+338_4852+339insTA	XP_005252029.1:n.4852+338_4852+339insTA
XM_005251973.2:c.4034-3731_4034-3730insTA	XP_005252030.1:n.4034-3731_4034-3730insTA
XM_005251974.2:c.3487+338_3487+339insTA	XP_005252031.1:n.3487+338_3487+339insTA
XM_005251975.2:c.3215-3731_3215-3730insTA	XP_005252032.1:n.3215-3731_3215-3730insTA
XM_006717096.2:c.5401+338_5401+339insTA	XP_006717159.1:n.5401+338_5401+339insTA
XM_006717097.2:c.4852+338_4852+339insTA	XP_006717160.1:n.4852+338_4852+339insTA
XM_006717098.2:c.4579+338_4579+339insTA	XP_006717161.1:n.4579+338_4579+339insTA
XM_006717100.2:c.4307-3731_4307-3730insTA	XP_006717163.1:n.4307-3731_4307-3730insTA
XM_006717101.2:c.3488-3731_3488-3730insTA	XP_006717164.1:n.3488-3731_3488-3730insTA
XM_011518622.1:c.5128+338_5128+339insTA	XP_011516924.1:n.5128+338_5128+339insTA
XM_011518623.1:c.5128+338_5128+339insTA	XP_011516925.1:n.5128+338_5128+339insTA
XM_011518624.1:c.4582+338_4582+339insTA	XP_011516926.1:n.4582+338_4582+339insTA
XM_011518625.1:c.4580-3731_4580-3730insTA	XP_011516927.1:n.4580-3731_4580-3730insTA
XM_011518626.1:c.4309+338_4309+339insTA	XP_011516928.1:n.4309+338_4309+339insTA
XM_011518627.1:c.4036+338_4036+339insTA	XP_011516929.1:n.4036+338_4036+339insTA
XM_011518628.1:c.3761-3731_3761-3730insTA	XP_011516930.1:n.3761-3731_3761-3730insTA
XM_011518629.1:c.3760+338_3760+339insTA	XP_011516931.1:n.3760+338_3760+339insTA
XM_005251972.4:c.4852+338_4852+339insTA	XP_005252029.1:n.4852+338_4852+339insTA
XM_005251973.4:c.4034-3731_4034-3730insTA	XP_005252030.1:n.4034-3731_4034-3730insTA
XM_005251974.4:c.3487+338_3487+339insTA	XP_005252031.1:n.3487+338_3487+339insTA
XM_005251975.4:c.3215-3731_3215-3730insTA	XP_005252032.1:n.3215-3731_3215-3730insTA
XM_006717096.4:c.5401+338_5401+339insTA	XP_006717159.1:n.5401+338_5401+339insTA
XM_006717097.4:c.4852+338_4852+339insTA	XP_006717160.1:n.4852+338_4852+339insTA
XM_006717098.4:c.4579+338_4579+339insTA	XP_006717161.1:n.4579+338_4579+339insTA
XM_006717101.4:c.3488-3731_3488-3730insTA	XP_006717164.1:n.3488-3731_3488-3730insTA
XM_011518625.3:c.4580-3731_4580-3730insTA	XP_011516927.1:n.4580-3731_4580-3730insTA
XM_011518626.3:c.4309+338_4309+339insTA	XP_011516928.1:n.4309+338_4309+339insTA
XM_011518628.3:c.3761-3731_3761-3730insTA	XP_011516930.1:n.3761-3731_3761-3730insTA
XM_011518629.3:c.3760+338_3760+339insTA	XP_011516931.1:n.3760+338_3760+339insTA
XM_017014678.2:c.5674+338_5674+339insTA	XP_016870167.1:n.5674+338_5674+339insTA
XM_017014679.2:c.5401+338_5401+339insTA	XP_016870168.1:n.5401+338_5401+339insTA
XM_017014680.2:c.5398+338_5398+339insTA	XP_016870169.1:n.5398+338_5398+339insTA
XM_017014681.2:c.4582+338_4582+339insTA	XP_016870170.1:n.4582+338_4582+339insTA
XM_024447530.1:c.5674+338_5674+339insTA	XP_024303298.1:n.5674+338_5674+339insTA
NM_002160.4:c.5125+338_5125+339insTA MANE Select	NP_002151.2:n.5125+338_5125+339insTA