Canonical Allele Identifier: CA2580617690

Gene: TANC2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63415676_63415677insTT , CM000679.2:g.63415676_63415677insTT	GRCh38
NC_000017.10:g.61493037_61493038insTT , CM000679.1:g.61493037_61493038insTT	GRCh37
NC_000017.9:g.58846769_58846770insTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001394998.1:c.4167+2_4167+3insTT MANE Select	NP_001381927.1:n.4167+2_4167+3insTT
ENST00000689528.1:c.4167+2_4167+3insTT MANE Select	ENSP00000510600.1:n.4167+2_4167+3insTT
NM_025185.3:c.3915+2_3915+3insTT	NP_079461.2:n.3915+2_3915+3insTT
NM_025185.4:c.3915+2_3915+3insTT	NP_079461.2:n.3915+2_3915+3insTT
ENST00000389520.8:c.3945+2_3945+3insTT	ENSP00000374171.4:n.3945+2_3945+3insTT
ENST00000424789.6:c.3915+2_3915+3insTT	ENSP00000387593.2:n.3915+2_3915+3insTT
ENST00000583356.5:c.3701+2_3701+3insTT
ENST00000613171.4:c.1245+2_1245+3insTT	ENSP00000478576.1:n.1245+2_1245+3insTT
XM_005257203.3:c.3915+2_3915+3insTT	XP_005257260.1:n.3915+2_3915+3insTT
XM_005257203.4:c.3915+2_3915+3insTT	XP_005257260.1:n.3915+2_3915+3insTT
XM_006721806.2:c.4167+2_4167+3insTT	XP_006721869.1:n.4167+2_4167+3insTT
XM_006721806.3:c.4167+2_4167+3insTT	XP_006721869.1:n.4167+2_4167+3insTT
XM_006721807.2:c.4137+2_4137+3insTT	XP_006721870.1:n.4137+2_4137+3insTT
XM_006721807.3:c.4137+2_4137+3insTT	XP_006721870.1:n.4137+2_4137+3insTT
XM_006721810.2:c.4167+2_4167+3insTT	XP_006721873.1:n.4167+2_4167+3insTT
XM_006721810.3:c.4167+2_4167+3insTT	XP_006721873.1:n.4167+2_4167+3insTT
XM_006721811.2:c.4137+2_4137+3insTT	XP_006721874.1:n.4137+2_4137+3insTT
XM_006721811.4:c.4137+2_4137+3insTT	XP_006721874.1:n.4137+2_4137+3insTT
XM_011524597.1:c.4167+2_4167+3insTT	XP_011522899.1:n.4167+2_4167+3insTT
XM_011524597.2:c.4167+2_4167+3insTT	XP_011522899.1:n.4167+2_4167+3insTT
XM_011524598.1:c.4137+2_4137+3insTT	XP_011522900.1:n.4137+2_4137+3insTT
XM_011524598.2:c.4137+2_4137+3insTT	XP_011522900.1:n.4137+2_4137+3insTT
XM_011524599.1:c.4119+2_4119+3insTT	XP_011522901.1:n.4119+2_4119+3insTT
XM_011524600.1:c.4056+2_4056+3insTT	XP_011522902.1:n.4056+2_4056+3insTT
XM_011524600.2:c.4056+2_4056+3insTT	XP_011522902.1:n.4056+2_4056+3insTT
XM_011524601.1:c.4056+2_4056+3insTT	XP_011522903.1:n.4056+2_4056+3insTT
XM_011524601.2:c.4056+2_4056+3insTT	XP_011522903.1:n.4056+2_4056+3insTT
XM_011524602.1:c.3945+2_3945+3insTT	XP_011522904.1:n.3945+2_3945+3insTT
XM_011524602.2:c.3945+2_3945+3insTT	XP_011522904.1:n.3945+2_3945+3insTT
XM_011524603.1:c.3675+2_3675+3insTT	XP_011522905.1:n.3675+2_3675+3insTT
XM_011524604.1:c.1017+2_1017+3insTT	XP_011522906.1:n.1017+2_1017+3insTT
XM_017024429.1:c.4089+2_4089+3insTT	XP_016879918.1:n.4089+2_4089+3insTT
XM_017024430.2:c.3675+2_3675+3insTT	XP_016879919.1:n.3675+2_3675+3insTT