Canonical Allele Identifier: CA357202735

Gene: ANKRD17

Linked Data

• MyVariant Identifiers: chr4:g.73942689A>G (hg19) ; chr4:g.73076972A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73076972A>G , CM000666.2:g.73076972A>G	GRCh38
NC_000004.11:g.73942689A>G , CM000666.1:g.73942689A>G	GRCh37
NC_000004.10:g.74161553A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358602.9:c.7720T>C MANE Select	ENSP00000351416.4:p.Ser2574Pro
ENST00000330838.10:c.6967T>C	ENSP00000332265.6:p.Ser2323Pro
ENST00000358602.8:c.7720T>C	ENSP00000351416.4:p.Ser2574Pro
ENST00000509867.6:c.7381T>C	ENSP00000427151.2:p.Ser2461Pro
ENST00000558247.5:c.7371T>C
NM_001286771.1:c.7381T>C	NP_001273700.1:p.Ser2461Pro
NM_032217.3:c.7720T>C	NP_115593.3:p.Ser2574Pro
NM_198889.1:c.6967T>C	NP_942592.1:p.Ser2323Pro
XM_005265667.3:c.7717T>C	XP_005265724.1:p.Ser2573Pro
XM_005265671.3:c.6964T>C	XP_005265728.1:p.Ser2322Pro
NM_001286771.2:c.7381T>C	NP_001273700.1:p.Ser2461Pro
NM_015574.1:c.7717T>C	NP_056389.1:p.Ser2573Pro
NM_032217.4:c.7720T>C	NP_115593.3:p.Ser2574Pro
NM_198889.2:c.6967T>C	NP_942592.1:p.Ser2323Pro
XM_005265671.4:c.6964T>C	XP_005265728.1:p.Ser2322Pro
XM_017008011.1:c.7378T>C	XP_016863500.1:p.Ser2460Pro
XM_017008012.1:c.6628T>C	XP_016863501.1:p.Ser2210Pro
XM_017008013.1:c.6625T>C	XP_016863502.1:p.Ser2209Pro
NM_001286771.3:c.7381T>C	NP_001273700.1:p.Ser2461Pro
NM_015574.2:c.7717T>C	NP_056389.1:p.Ser2573Pro
NM_032217.5:c.7720T>C MANE Select	NP_115593.3:p.Ser2574Pro
NM_198889.3:c.6967T>C	NP_942592.1:p.Ser2323Pro