Canonical Allele Identifier: CA1467995715

Gene: ANKRD17

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73076811C= , CM000666.2:g.73076811C=	GRCh38
NC_000004.11:g.73942528C= , CM000666.1:g.73942528C=	GRCh37
NC_000004.10:g.74161392C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358602.9:c.7752+129G= MANE Select	ENSP00000351416.4:n.7752+129G=
ENST00000330838.10:c.6999+129G=	ENSP00000332265.6:n.6999+129G=
ENST00000358602.8:c.7752+129G=	ENSP00000351416.4:n.7752+129G=
ENST00000509867.6:c.7413+129G=	ENSP00000427151.2:n.7413+129G=
ENST00000558247.5:c.7403+129G=
NM_001286771.1:c.7413+129G=	NP_001273700.1:n.7413+129G=
NM_032217.3:c.7752+129G=	NP_115593.3:n.7752+129G=
NM_198889.1:c.6999+129G=	NP_942592.1:n.6999+129G=
XM_005265667.3:c.7749+129G=	XP_005265724.1:n.7749+129G=
XM_005265671.3:c.6996+129G=	XP_005265728.1:n.6996+129G=
NM_001286771.2:c.7413+129G=	NP_001273700.1:n.7413+129G=
NM_015574.1:c.7749+129G=	NP_056389.1:n.7749+129G=
NM_032217.4:c.7752+129G=	NP_115593.3:n.7752+129G=
NM_198889.2:c.6999+129G=	NP_942592.1:n.6999+129G=
XM_005265671.4:c.6996+129G=	XP_005265728.1:n.6996+129G=
XM_017008011.1:c.7410+129G=	XP_016863500.1:n.7410+129G=
XM_017008012.1:c.6660+129G=	XP_016863501.1:n.6660+129G=
XM_017008013.1:c.6657+129G=	XP_016863502.1:n.6657+129G=
NM_001286771.3:c.7413+129G=	NP_001273700.1:n.7413+129G=
NM_015574.2:c.7749+129G=	NP_056389.1:n.7749+129G=
NM_032217.5:c.7752+129G= MANE Select	NP_115593.3:n.7752+129G=
NM_198889.3:c.6999+129G=	NP_942592.1:n.6999+129G=