Canonical Allele Identifier: CA2706388230

Gene: ANKRD17

Linked Data

• dbSNP Id: rs2110079520

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73076965del , CM000666.2:g.73076965del	GRCh38
NC_000004.11:g.73942682del , CM000666.1:g.73942682del	GRCh37
NC_000004.10:g.74161546del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358602.9:c.7728del MANE Select	ENSP00000351416.4:p.Thr2577ArgfsTer18
ENST00000330838.10:c.6975del	ENSP00000332265.6:p.Thr2326ArgfsTer18
ENST00000358602.8:c.7728del	ENSP00000351416.4:p.Thr2577ArgfsTer18
ENST00000509867.6:c.7389del	ENSP00000427151.2:p.Thr2464ArgfsTer18
ENST00000558247.5:c.7379del
NM_001286771.1:c.7389del	NP_001273700.1:p.Thr2464ArgfsTer18
NM_032217.3:c.7728del	NP_115593.3:p.Thr2577ArgfsTer18
NM_198889.1:c.6975del	NP_942592.1:p.Thr2326ArgfsTer18
XM_005265667.3:c.7725del	XP_005265724.1:p.Thr2576ArgfsTer18
XM_005265671.3:c.6972del	XP_005265728.1:p.Thr2325ArgfsTer18
NM_001286771.2:c.7389del	NP_001273700.1:p.Thr2464ArgfsTer18
NM_015574.1:c.7725del	NP_056389.1:p.Thr2576ArgfsTer18
NM_032217.4:c.7728del	NP_115593.3:p.Thr2577ArgfsTer18
NM_198889.2:c.6975del	NP_942592.1:p.Thr2326ArgfsTer18
XM_005265671.4:c.6972del	XP_005265728.1:p.Thr2325ArgfsTer18
XM_017008011.1:c.7386del	XP_016863500.1:p.Thr2463ArgfsTer18
XM_017008012.1:c.6636del	XP_016863501.1:p.Thr2213ArgfsTer18
XM_017008013.1:c.6633del	XP_016863502.1:p.Thr2212ArgfsTer18
NM_001286771.3:c.7389del	NP_001273700.1:p.Thr2464ArgfsTer18
NM_015574.2:c.7725del	NP_056389.1:p.Thr2576ArgfsTer18
NM_032217.5:c.7728del MANE Select	NP_115593.3:p.Thr2577ArgfsTer18
NM_198889.3:c.6975del	NP_942592.1:p.Thr2326ArgfsTer18