Canonical Allele Identifier: CA439797850

Gene: ANKRD17

Linked Data

• MyVariant Identifiers: chr4:g.73942687G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73076970G>C , CM000666.2:g.73076970G>C	GRCh38
NC_000004.11:g.73942687G>C , CM000666.1:g.73942687G>C	GRCh37
NC_000004.10:g.74161551G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358602.9:c.7722C>G MANE Select	ENSP00000351416.4:p.Ser2574=
ENST00000330838.10:c.6969C>G	ENSP00000332265.6:p.Ser2323=
ENST00000358602.8:c.7722C>G	ENSP00000351416.4:p.Ser2574=
ENST00000509867.6:c.7383C>G	ENSP00000427151.2:p.Ser2461=
ENST00000558247.5:c.7373C>G
NM_001286771.1:c.7383C>G	NP_001273700.1:p.Ser2461=
NM_032217.3:c.7722C>G	NP_115593.3:p.Ser2574=
NM_198889.1:c.6969C>G	NP_942592.1:p.Ser2323=
XM_005265667.3:c.7719C>G	XP_005265724.1:p.Ser2573=
XM_005265671.3:c.6966C>G	XP_005265728.1:p.Ser2322=
NM_001286771.2:c.7383C>G	NP_001273700.1:p.Ser2461=
NM_015574.1:c.7719C>G	NP_056389.1:p.Ser2573=
NM_032217.4:c.7722C>G	NP_115593.3:p.Ser2574=
NM_198889.2:c.6969C>G	NP_942592.1:p.Ser2323=
XM_005265671.4:c.6966C>G	XP_005265728.1:p.Ser2322=
XM_017008011.1:c.7380C>G	XP_016863500.1:p.Ser2460=
XM_017008012.1:c.6630C>G	XP_016863501.1:p.Ser2210=
XM_017008013.1:c.6627C>G	XP_016863502.1:p.Ser2209=
NM_001286771.3:c.7383C>G	NP_001273700.1:p.Ser2461=
NM_015574.2:c.7719C>G	NP_056389.1:p.Ser2573=
NM_032217.5:c.7722C>G MANE Select	NP_115593.3:p.Ser2574=
NM_198889.3:c.6969C>G	NP_942592.1:p.Ser2323=