Canonical Allele Identifier: CA357202643

Gene: ANKRD17

Linked Data

• MyVariant Identifiers: chr4:g.73942679G>C (hg19) ; chr4:g.73076962G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000358602.9:c.7730C>G MANE Select	ENSP00000351416.4:p.Thr2577Arg
ENST00000330838.10:c.6977C>G	ENSP00000332265.6:p.Thr2326Arg
ENST00000358602.8:c.7730C>G	ENSP00000351416.4:p.Thr2577Arg
ENST00000509867.6:c.7391C>G	ENSP00000427151.2:p.Thr2464Arg
ENST00000558247.5:c.7381C>G
NM_001286771.1:c.7391C>G	NP_001273700.1:p.Thr2464Arg
NM_032217.3:c.7730C>G	NP_115593.3:p.Thr2577Arg
NM_198889.1:c.6977C>G	NP_942592.1:p.Thr2326Arg
XM_005265667.3:c.7727C>G	XP_005265724.1:p.Thr2576Arg
XM_005265671.3:c.6974C>G	XP_005265728.1:p.Thr2325Arg
NM_001286771.2:c.7391C>G	NP_001273700.1:p.Thr2464Arg
NM_015574.1:c.7727C>G	NP_056389.1:p.Thr2576Arg
NM_032217.4:c.7730C>G	NP_115593.3:p.Thr2577Arg
NM_198889.2:c.6977C>G	NP_942592.1:p.Thr2326Arg
XM_005265671.4:c.6974C>G	XP_005265728.1:p.Thr2325Arg
XM_017008011.1:c.7388C>G	XP_016863500.1:p.Thr2463Arg
XM_017008012.1:c.6638C>G	XP_016863501.1:p.Thr2213Arg
XM_017008013.1:c.6635C>G	XP_016863502.1:p.Thr2212Arg
NM_001286771.3:c.7391C>G	NP_001273700.1:p.Thr2464Arg
NM_015574.2:c.7727C>G	NP_056389.1:p.Thr2576Arg
NM_032217.5:c.7730C>G MANE Select	NP_115593.3:p.Thr2577Arg
NM_198889.3:c.6977C>G	NP_942592.1:p.Thr2326Arg