Canonical Allele Identifier: CA798227618

Gene: ANKRD17

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73104747C>G , CM000666.2:g.73104747C>G	GRCh38
NC_000004.11:g.73970464C>G , CM000666.1:g.73970464C>G	GRCh37
NC_000004.10:g.74189328C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358602.9:c.4402-2200G>C MANE Select	ENSP00000351416.4:n.4402-2200G>C
ENST00000330838.10:c.3649-2200G>C	ENSP00000332265.6:n.3649-2200G>C
ENST00000358602.8:c.4402-2200G>C	ENSP00000351416.4:n.4402-2200G>C
ENST00000509867.6:c.4063-2200G>C	ENSP00000427151.2:n.4063-2200G>C
ENST00000558247.5:c.4053-2200G>C
ENST00000561029.1:c.2503-2200G>C	ENSP00000453294.1:n.2503-2200G>C
NM_001286771.1:c.4063-2200G>C	NP_001273700.1:n.4063-2200G>C
NM_032217.3:c.4402-2200G>C	NP_115593.3:n.4402-2200G>C
NM_198889.1:c.3649-2200G>C	NP_942592.1:n.3649-2200G>C
XM_005265667.3:c.4399-2200G>C	XP_005265724.1:n.4399-2200G>C
XM_005265671.3:c.3646-2200G>C	XP_005265728.1:n.3646-2200G>C
XM_005265672.3:c.4402-2200G>C	XP_005265729.1:n.4402-2200G>C
NM_001286771.2:c.4063-2200G>C	NP_001273700.1:n.4063-2200G>C
NM_015574.1:c.4399-2200G>C	NP_056389.1:n.4399-2200G>C
NM_032217.4:c.4402-2200G>C	NP_115593.3:n.4402-2200G>C
NM_198889.2:c.3649-2200G>C	NP_942592.1:n.3649-2200G>C
XM_005265671.4:c.3646-2200G>C	XP_005265728.1:n.3646-2200G>C
XM_005265672.4:c.4402-2200G>C	XP_005265729.1:n.4402-2200G>C
XM_017008011.1:c.4060-2200G>C	XP_016863500.1:n.4060-2200G>C
XM_017008012.1:c.3310-2200G>C	XP_016863501.1:n.3310-2200G>C
XM_017008013.1:c.3307-2200G>C	XP_016863502.1:n.3307-2200G>C
NM_001286771.3:c.4063-2200G>C	NP_001273700.1:n.4063-2200G>C
NM_015574.2:c.4399-2200G>C	NP_056389.1:n.4399-2200G>C
NM_032217.5:c.4402-2200G>C MANE Select	NP_115593.3:n.4402-2200G>C
NM_198889.3:c.3649-2200G>C	NP_942592.1:n.3649-2200G>C