Canonical Allele Identifier: CA1467995780

Gene: ANKRD17

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73076962G= , CM000666.2:g.73076962G=	GRCh38
NC_000004.11:g.73942679G= , CM000666.1:g.73942679G=	GRCh37
NC_000004.10:g.74161543G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358602.9:c.7730C= MANE Select	ENSP00000351416.4:p.Thr2577=
ENST00000330838.10:c.6977C=	ENSP00000332265.6:p.Thr2326=
ENST00000358602.8:c.7730C=	ENSP00000351416.4:p.Thr2577=
ENST00000509867.6:c.7391C=	ENSP00000427151.2:p.Thr2464=
ENST00000558247.5:c.7381C=
NM_001286771.1:c.7391C=	NP_001273700.1:p.Thr2464=
NM_032217.3:c.7730C=	NP_115593.3:p.Thr2577=
NM_198889.1:c.6977C=	NP_942592.1:p.Thr2326=
XM_005265667.3:c.7727C=	XP_005265724.1:p.Thr2576=
XM_005265671.3:c.6974C=	XP_005265728.1:p.Thr2325=
NM_001286771.2:c.7391C=	NP_001273700.1:p.Thr2464=
NM_015574.1:c.7727C=	NP_056389.1:p.Thr2576=
NM_032217.4:c.7730C=	NP_115593.3:p.Thr2577=
NM_198889.2:c.6977C=	NP_942592.1:p.Thr2326=
XM_005265671.4:c.6974C=	XP_005265728.1:p.Thr2325=
XM_017008011.1:c.7388C=	XP_016863500.1:p.Thr2463=
XM_017008012.1:c.6638C=	XP_016863501.1:p.Thr2213=
XM_017008013.1:c.6635C=	XP_016863502.1:p.Thr2212=
NM_001286771.3:c.7391C=	NP_001273700.1:p.Thr2464=
NM_015574.2:c.7727C=	NP_056389.1:p.Thr2576=
NM_032217.5:c.7730C= MANE Select	NP_115593.3:p.Thr2577=
NM_198889.3:c.6977C=	NP_942592.1:p.Thr2326=