Canonical Allele Identifier: CA357202719
Gene: ANKRD17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73076971G>A , CM000666.2:g.73076971G>A GRCh38
NC_000004.11:g.73942688G>A , CM000666.1:g.73942688G>A GRCh37
NC_000004.10:g.74161552G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000358602.9:c.7721C>T MANE Select ENSP00000351416.4:p.Ser2574Phe
ENST00000330838.10:c.6968C>T ENSP00000332265.6:p.Ser2323Phe
ENST00000358602.8:c.7721C>T ENSP00000351416.4:p.Ser2574Phe
ENST00000509867.6:c.7382C>T ENSP00000427151.2:p.Ser2461Phe
ENST00000558247.5:c.7372C>T
NM_001286771.1:c.7382C>T NP_001273700.1:p.Ser2461Phe
NM_032217.3:c.7721C>T NP_115593.3:p.Ser2574Phe
NM_198889.1:c.6968C>T NP_942592.1:p.Ser2323Phe
XM_005265667.3:c.7718C>T XP_005265724.1:p.Ser2573Phe
XM_005265671.3:c.6965C>T XP_005265728.1:p.Ser2322Phe
NM_001286771.2:c.7382C>T NP_001273700.1:p.Ser2461Phe
NM_015574.1:c.7718C>T NP_056389.1:p.Ser2573Phe
NM_032217.4:c.7721C>T NP_115593.3:p.Ser2574Phe
NM_198889.2:c.6968C>T NP_942592.1:p.Ser2323Phe
XM_005265671.4:c.6965C>T XP_005265728.1:p.Ser2322Phe
XM_017008011.1:c.7379C>T XP_016863500.1:p.Ser2460Phe
XM_017008012.1:c.6629C>T XP_016863501.1:p.Ser2210Phe
XM_017008013.1:c.6626C>T XP_016863502.1:p.Ser2209Phe
NM_001286771.3:c.7382C>T NP_001273700.1:p.Ser2461Phe
NM_015574.2:c.7718C>T NP_056389.1:p.Ser2573Phe
NM_032217.5:c.7721C>T MANE Select NP_115593.3:p.Ser2574Phe
NM_198889.3:c.6968C>T NP_942592.1:p.Ser2323Phe