Canonical Allele Identifier: CA2580094541

Gene: TANC2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63314672A>G , CM000679.2:g.63314672A>G	GRCh38
NC_000017.10:g.61392033A>G , CM000679.1:g.61392033A>G	GRCh37
NC_000017.9:g.58745765A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001394998.1:c.1441+3A>G MANE Select	NP_001381927.1:n.1441+3A>G
ENST00000689528.1:c.1441+3A>G MANE Select	ENSP00000510600.1:n.1441+3A>G
NM_025185.3:c.1219+3A>G	NP_079461.2:n.1219+3A>G
NM_025185.4:c.1219+3A>G	NP_079461.2:n.1219+3A>G
ENST00000389520.8:c.1219+3A>G	ENSP00000374171.4:n.1219+3A>G
ENST00000424789.6:c.1219+3A>G	ENSP00000387593.2:n.1219+3A>G
ENST00000583356.5:c.1005+3A>G
XM_005257203.3:c.1219+3A>G	XP_005257260.1:n.1219+3A>G
XM_005257203.4:c.1219+3A>G	XP_005257260.1:n.1219+3A>G
XM_006721806.2:c.1441+3A>G	XP_006721869.1:n.1441+3A>G
XM_006721806.3:c.1441+3A>G	XP_006721869.1:n.1441+3A>G
XM_006721807.2:c.1441+3A>G	XP_006721870.1:n.1441+3A>G
XM_006721807.3:c.1441+3A>G	XP_006721870.1:n.1441+3A>G
XM_006721810.2:c.1441+3A>G	XP_006721873.1:n.1441+3A>G
XM_006721810.3:c.1441+3A>G	XP_006721873.1:n.1441+3A>G
XM_006721811.2:c.1441+3A>G	XP_006721874.1:n.1441+3A>G
XM_006721811.4:c.1441+3A>G	XP_006721874.1:n.1441+3A>G
XM_011524597.1:c.1441+3A>G	XP_011522899.1:n.1441+3A>G
XM_011524597.2:c.1441+3A>G	XP_011522899.1:n.1441+3A>G
XM_011524598.1:c.1441+3A>G	XP_011522900.1:n.1441+3A>G
XM_011524598.2:c.1441+3A>G	XP_011522900.1:n.1441+3A>G
XM_011524599.1:c.1393+3A>G	XP_011522901.1:n.1393+3A>G
XM_011524600.1:c.1330+3A>G	XP_011522902.1:n.1330+3A>G
XM_011524600.2:c.1330+3A>G	XP_011522902.1:n.1330+3A>G
XM_011524601.1:c.1330+3A>G	XP_011522903.1:n.1330+3A>G
XM_011524601.2:c.1330+3A>G	XP_011522903.1:n.1330+3A>G
XM_011524602.1:c.1219+3A>G	XP_011522904.1:n.1219+3A>G
XM_011524602.2:c.1219+3A>G	XP_011522904.1:n.1219+3A>G
XM_011524603.1:c.949+3A>G	XP_011522905.1:n.949+3A>G
XM_017024429.1:c.1393+3A>G	XP_016879918.1:n.1393+3A>G
XM_017024430.2:c.949+3A>G	XP_016879919.1:n.949+3A>G
XM_017024431.1:c.1441+3A>G	XP_016879920.1:n.1441+3A>G