Canonical Allele Identifier: CA439797838

Gene: ANKRD17

Linked Data

• MyVariant Identifiers: chr4:g.73942681G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73076964G>T , CM000666.2:g.73076964G>T	GRCh38
NC_000004.11:g.73942681G>T , CM000666.1:g.73942681G>T	GRCh37
NC_000004.10:g.74161545G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358602.9:c.7728C>A MANE Select	ENSP00000351416.4:p.Ser2576=
ENST00000330838.10:c.6975C>A	ENSP00000332265.6:p.Ser2325=
ENST00000358602.8:c.7728C>A	ENSP00000351416.4:p.Ser2576=
ENST00000509867.6:c.7389C>A	ENSP00000427151.2:p.Ser2463=
ENST00000558247.5:c.7379C>A
NM_001286771.1:c.7389C>A	NP_001273700.1:p.Ser2463=
NM_032217.3:c.7728C>A	NP_115593.3:p.Ser2576=
NM_198889.1:c.6975C>A	NP_942592.1:p.Ser2325=
XM_005265667.3:c.7725C>A	XP_005265724.1:p.Ser2575=
XM_005265671.3:c.6972C>A	XP_005265728.1:p.Ser2324=
NM_001286771.2:c.7389C>A	NP_001273700.1:p.Ser2463=
NM_015574.1:c.7725C>A	NP_056389.1:p.Ser2575=
NM_032217.4:c.7728C>A	NP_115593.3:p.Ser2576=
NM_198889.2:c.6975C>A	NP_942592.1:p.Ser2325=
XM_005265671.4:c.6972C>A	XP_005265728.1:p.Ser2324=
XM_017008011.1:c.7386C>A	XP_016863500.1:p.Ser2462=
XM_017008012.1:c.6636C>A	XP_016863501.1:p.Ser2212=
XM_017008013.1:c.6633C>A	XP_016863502.1:p.Ser2211=
NM_001286771.3:c.7389C>A	NP_001273700.1:p.Ser2463=
NM_015574.2:c.7725C>A	NP_056389.1:p.Ser2575=
NM_032217.5:c.7728C>A MANE Select	NP_115593.3:p.Ser2576=
NM_198889.3:c.6975C>A	NP_942592.1:p.Ser2325=