Canonical Allele Identifier: CA439797856

Gene: ANKRD17

Linked Data

• MyVariant Identifiers: chr4:g.73942690A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73076973A>G , CM000666.2:g.73076973A>G	GRCh38
NC_000004.11:g.73942690A>G , CM000666.1:g.73942690A>G	GRCh37
NC_000004.10:g.74161554A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358602.9:c.7719T>C MANE Select	ENSP00000351416.4:p.Val2573=
ENST00000330838.10:c.6966T>C	ENSP00000332265.6:p.Val2322=
ENST00000358602.8:c.7719T>C	ENSP00000351416.4:p.Val2573=
ENST00000509867.6:c.7380T>C	ENSP00000427151.2:p.Val2460=
ENST00000558247.5:c.7370T>C
NM_001286771.1:c.7380T>C	NP_001273700.1:p.Val2460=
NM_032217.3:c.7719T>C	NP_115593.3:p.Val2573=
NM_198889.1:c.6966T>C	NP_942592.1:p.Val2322=
XM_005265667.3:c.7716T>C	XP_005265724.1:p.Val2572=
XM_005265671.3:c.6963T>C	XP_005265728.1:p.Val2321=
NM_001286771.2:c.7380T>C	NP_001273700.1:p.Val2460=
NM_015574.1:c.7716T>C	NP_056389.1:p.Val2572=
NM_032217.4:c.7719T>C	NP_115593.3:p.Val2573=
NM_198889.2:c.6966T>C	NP_942592.1:p.Val2322=
XM_005265671.4:c.6963T>C	XP_005265728.1:p.Val2321=
XM_017008011.1:c.7377T>C	XP_016863500.1:p.Val2459=
XM_017008012.1:c.6627T>C	XP_016863501.1:p.Val2209=
XM_017008013.1:c.6624T>C	XP_016863502.1:p.Val2208=
NM_001286771.3:c.7380T>C	NP_001273700.1:p.Val2460=
NM_015574.2:c.7716T>C	NP_056389.1:p.Val2572=
NM_032217.5:c.7719T>C MANE Select	NP_115593.3:p.Val2573=
NM_198889.3:c.6966T>C	NP_942592.1:p.Val2322=