Canonical Allele Identifier: CA798277498

Gene: ANKRD17

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73189781G>T , CM000666.2:g.73189781G>T	GRCh38
NC_000004.11:g.74055498G>T , CM000666.1:g.74055498G>T	GRCh37
NC_000004.10:g.74274362G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358602.9:c.394-12248C>A MANE Select	ENSP00000351416.4:n.394-12248C>A
ENST00000639793.1:c.394-12248C>A	ENSP00000491481.1:n.394-12248C>A
ENST00000330838.10:c.394-12248C>A	ENSP00000332265.6:n.394-12248C>A
ENST00000358602.8:c.394-12248C>A	ENSP00000351416.4:n.394-12248C>A
ENST00000509867.6:c.55-12248C>A	ENSP00000427151.2:n.55-12248C>A
ENST00000558247.5:c.48-12248C>A
ENST00000559367.1:n.67-12248C>A
ENST00000561029.1:c.385-47989C>A	ENSP00000453294.1:n.385-47989C>A
NM_001286771.1:c.55-12248C>A	NP_001273700.1:n.55-12248C>A
NM_032217.3:c.394-12248C>A	NP_115593.3:n.394-12248C>A
NM_198889.1:c.394-12248C>A	NP_942592.1:n.394-12248C>A
XM_005265667.3:c.394-12248C>A	XP_005265724.1:n.394-12248C>A
XM_005265671.3:c.394-12248C>A	XP_005265728.1:n.394-12248C>A
XM_005265672.3:c.394-12248C>A	XP_005265729.1:n.394-12248C>A
XM_005265673.2:c.394-12248C>A	XP_005265730.1:n.394-12248C>A
NM_001286771.2:c.55-12248C>A	NP_001273700.1:n.55-12248C>A
NM_015574.1:c.394-12248C>A	NP_056389.1:n.394-12248C>A
NM_032217.4:c.394-12248C>A	NP_115593.3:n.394-12248C>A
NM_198889.2:c.394-12248C>A	NP_942592.1:n.394-12248C>A
XM_005265671.4:c.394-12248C>A	XP_005265728.1:n.394-12248C>A
XM_005265672.4:c.394-12248C>A	XP_005265729.1:n.394-12248C>A
XM_005265673.4:c.394-12248C>A	XP_005265730.1:n.394-12248C>A
XM_017008011.1:c.55-12248C>A	XP_016863500.1:n.55-12248C>A
XM_017008012.1:c.55-12248C>A	XP_016863501.1:n.55-12248C>A
XM_017008013.1:c.55-12248C>A	XP_016863502.1:n.55-12248C>A
XM_017008014.2:c.394-12248C>A	XP_016863503.1:n.394-12248C>A
XM_017008015.1:c.55-12248C>A	XP_016863504.1:n.55-12248C>A
XM_017008016.2:c.394-12248C>A	XP_016863505.1:n.394-12248C>A
XM_017008017.1:c.55-12248C>A	XP_016863506.1:n.55-12248C>A
NM_001286771.3:c.55-12248C>A	NP_001273700.1:n.55-12248C>A
NM_015574.2:c.394-12248C>A	NP_056389.1:n.394-12248C>A
NM_032217.5:c.394-12248C>A MANE Select	NP_115593.3:n.394-12248C>A
NM_198889.3:c.394-12248C>A	NP_942592.1:n.394-12248C>A