Canonical Allele Identifier: CA293240350

Gene: TANC2

Linked Data

• dbSNP Id: rs150281743
• gnomAD v2: 17-61045111-C-A
• gnomAD v3: 17-62967750-C-A
• gnomAD v4: 17-62967750-C-A
• MyVariant Identifiers: chr17:g.61045111C>A (hg19) ; chr17:g.62967750C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.62967750C>A , CM000679.2:g.62967750C>A	GRCh38
NC_000017.10:g.61045111C>A , CM000679.1:g.61045111C>A	GRCh37
NC_000017.9:g.58398843C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689528.1:c.-24+1001C>A MANE Select	ENSP00000510600.1:n.-24+1001C>A
XM_005257203.3:c.-24+1001C>A	XP_005257260.1:n.-24+1001C>A
XM_006721806.2:c.-24+1001C>A	XP_006721869.1:n.-24+1001C>A
XM_006721807.2:c.-24+1001C>A	XP_006721870.1:n.-24+1001C>A
XM_006721810.2:c.-24+1001C>A	XP_006721873.1:n.-24+1001C>A
XM_006721811.2:c.-24+1001C>A	XP_006721874.1:n.-24+1001C>A
XM_011524597.1:c.-24+1001C>A	XP_011522899.1:n.-24+1001C>A
XM_011524598.1:c.-24+1001C>A	XP_011522900.1:n.-24+1001C>A
XM_011524600.1:c.-24+1001C>A	XP_011522902.1:n.-24+1001C>A
XM_011524601.1:c.-24+1001C>A	XP_011522903.1:n.-24+1001C>A
XM_011524602.1:c.-24+1001C>A	XP_011522904.1:n.-24+1001C>A
XM_005257203.4:c.-24+1001C>A	XP_005257260.1:n.-24+1001C>A
XM_006721806.3:c.-24+1001C>A	XP_006721869.1:n.-24+1001C>A
XM_006721807.3:c.-24+1001C>A	XP_006721870.1:n.-24+1001C>A
XM_006721810.3:c.-24+1001C>A	XP_006721873.1:n.-24+1001C>A
XM_006721811.4:c.-24+1001C>A	XP_006721874.1:n.-24+1001C>A
XM_011524597.2:c.-24+1001C>A	XP_011522899.1:n.-24+1001C>A
XM_011524598.2:c.-24+1001C>A	XP_011522900.1:n.-24+1001C>A
XM_011524600.2:c.-24+1001C>A	XP_011522902.1:n.-24+1001C>A
XM_011524601.2:c.-24+1001C>A	XP_011522903.1:n.-24+1001C>A
XM_011524602.2:c.-24+1001C>A	XP_011522904.1:n.-24+1001C>A
XM_017024431.1:c.-24+1001C>A	XP_016879920.1:n.-24+1001C>A
NM_025185.4:c.-24+1001C>A	NP_079461.2:n.-24+1001C>A
NM_001394998.1:c.-24+1001C>A MANE Select	NP_001381927.1:n.-24+1001C>A