Canonical Allele Identifier: CA357202746

Gene: ANKRD17

Linked Data

• MyVariant Identifiers: chr4:g.73942691A>G (hg19) ; chr4:g.73076974A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73076974A>G , CM000666.2:g.73076974A>G	GRCh38
NC_000004.11:g.73942691A>G , CM000666.1:g.73942691A>G	GRCh37
NC_000004.10:g.74161555A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358602.9:c.7718T>C MANE Select	ENSP00000351416.4:p.Val2573Ala
ENST00000330838.10:c.6965T>C	ENSP00000332265.6:p.Val2322Ala
ENST00000358602.8:c.7718T>C	ENSP00000351416.4:p.Val2573Ala
ENST00000509867.6:c.7379T>C	ENSP00000427151.2:p.Val2460Ala
ENST00000558247.5:c.7369T>C
NM_001286771.1:c.7379T>C	NP_001273700.1:p.Val2460Ala
NM_032217.3:c.7718T>C	NP_115593.3:p.Val2573Ala
NM_198889.1:c.6965T>C	NP_942592.1:p.Val2322Ala
XM_005265667.3:c.7715T>C	XP_005265724.1:p.Val2572Ala
XM_005265671.3:c.6962T>C	XP_005265728.1:p.Val2321Ala
NM_001286771.2:c.7379T>C	NP_001273700.1:p.Val2460Ala
NM_015574.1:c.7715T>C	NP_056389.1:p.Val2572Ala
NM_032217.4:c.7718T>C	NP_115593.3:p.Val2573Ala
NM_198889.2:c.6965T>C	NP_942592.1:p.Val2322Ala
XM_005265671.4:c.6962T>C	XP_005265728.1:p.Val2321Ala
XM_017008011.1:c.7376T>C	XP_016863500.1:p.Val2459Ala
XM_017008012.1:c.6626T>C	XP_016863501.1:p.Val2209Ala
XM_017008013.1:c.6623T>C	XP_016863502.1:p.Val2208Ala
NM_001286771.3:c.7379T>C	NP_001273700.1:p.Val2460Ala
NM_015574.2:c.7715T>C	NP_056389.1:p.Val2572Ala
NM_032217.5:c.7718T>C MANE Select	NP_115593.3:p.Val2573Ala
NM_198889.3:c.6965T>C	NP_942592.1:p.Val2322Ala