Canonical Allele Identifier: CA357202359

Gene: ANKRD17

Linked Data

• MyVariant Identifiers: chr4:g.73942655A>C (hg19) ; chr4:g.73076938A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73076938A>C , CM000666.2:g.73076938A>C	GRCh38
NC_000004.11:g.73942655A>C , CM000666.1:g.73942655A>C	GRCh37
NC_000004.10:g.74161519A>C	NCBI36

Transcript Alleles

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