Canonical Allele Identifier: CA1467995771
Gene: ANKRD17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73076929A= , CM000666.2:g.73076929A= GRCh38
NC_000004.11:g.73942646A= , CM000666.1:g.73942646A= GRCh37
NC_000004.10:g.74161510A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000358602.9:c.7752+11T= MANE Select ENSP00000351416.4:n.7752+11T=
ENST00000330838.10:c.6999+11T= ENSP00000332265.6:n.6999+11T=
ENST00000358602.8:c.7752+11T= ENSP00000351416.4:n.7752+11T=
ENST00000509867.6:c.7413+11T= ENSP00000427151.2:n.7413+11T=
ENST00000558247.5:c.7403+11T=
NM_001286771.1:c.7413+11T= NP_001273700.1:n.7413+11T=
NM_032217.3:c.7752+11T= NP_115593.3:n.7752+11T=
NM_198889.1:c.6999+11T= NP_942592.1:n.6999+11T=
XM_005265667.3:c.7749+11T= XP_005265724.1:n.7749+11T=
XM_005265671.3:c.6996+11T= XP_005265728.1:n.6996+11T=
NM_001286771.2:c.7413+11T= NP_001273700.1:n.7413+11T=
NM_015574.1:c.7749+11T= NP_056389.1:n.7749+11T=
NM_032217.4:c.7752+11T= NP_115593.3:n.7752+11T=
NM_198889.2:c.6999+11T= NP_942592.1:n.6999+11T=
XM_005265671.4:c.6996+11T= XP_005265728.1:n.6996+11T=
XM_017008011.1:c.7410+11T= XP_016863500.1:n.7410+11T=
XM_017008012.1:c.6660+11T= XP_016863501.1:n.6660+11T=
XM_017008013.1:c.6657+11T= XP_016863502.1:n.6657+11T=
NM_001286771.3:c.7413+11T= NP_001273700.1:n.7413+11T=
NM_015574.2:c.7749+11T= NP_056389.1:n.7749+11T=
NM_032217.5:c.7752+11T= MANE Select NP_115593.3:n.7752+11T=
NM_198889.3:c.6999+11T= NP_942592.1:n.6999+11T=