Canonical Allele Identifier: CA357202672

Gene: ANKRD17

Linked Data

• MyVariant Identifiers: chr4:g.73942682G>A (hg19) ; chr4:g.73076965G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73076965G>A , CM000666.2:g.73076965G>A	GRCh38
NC_000004.11:g.73942682G>A , CM000666.1:g.73942682G>A	GRCh37
NC_000004.10:g.74161546G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358602.9:c.7727C>T MANE Select	ENSP00000351416.4:p.Ser2576Phe
ENST00000330838.10:c.6974C>T	ENSP00000332265.6:p.Ser2325Phe
ENST00000358602.8:c.7727C>T	ENSP00000351416.4:p.Ser2576Phe
ENST00000509867.6:c.7388C>T	ENSP00000427151.2:p.Ser2463Phe
ENST00000558247.5:c.7378C>T
NM_001286771.1:c.7388C>T	NP_001273700.1:p.Ser2463Phe
NM_032217.3:c.7727C>T	NP_115593.3:p.Ser2576Phe
NM_198889.1:c.6974C>T	NP_942592.1:p.Ser2325Phe
XM_005265667.3:c.7724C>T	XP_005265724.1:p.Ser2575Phe
XM_005265671.3:c.6971C>T	XP_005265728.1:p.Ser2324Phe
NM_001286771.2:c.7388C>T	NP_001273700.1:p.Ser2463Phe
NM_015574.1:c.7724C>T	NP_056389.1:p.Ser2575Phe
NM_032217.4:c.7727C>T	NP_115593.3:p.Ser2576Phe
NM_198889.2:c.6974C>T	NP_942592.1:p.Ser2325Phe
XM_005265671.4:c.6971C>T	XP_005265728.1:p.Ser2324Phe
XM_017008011.1:c.7385C>T	XP_016863500.1:p.Ser2462Phe
XM_017008012.1:c.6635C>T	XP_016863501.1:p.Ser2212Phe
XM_017008013.1:c.6632C>T	XP_016863502.1:p.Ser2211Phe
NM_001286771.3:c.7388C>T	NP_001273700.1:p.Ser2463Phe
NM_015574.2:c.7724C>T	NP_056389.1:p.Ser2575Phe
NM_032217.5:c.7727C>T MANE Select	NP_115593.3:p.Ser2576Phe
NM_198889.3:c.6974C>T	NP_942592.1:p.Ser2325Phe