Canonical Allele Identifier: CA357202680

Gene: ANKRD17

Linked Data

• MyVariant Identifiers: chr4:g.73942683A>C (hg19) ; chr4:g.73076966A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73076966A>C , CM000666.2:g.73076966A>C	GRCh38
NC_000004.11:g.73942683A>C , CM000666.1:g.73942683A>C	GRCh37
NC_000004.10:g.74161547A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358602.9:c.7726T>G MANE Select	ENSP00000351416.4:p.Ser2576Ala
ENST00000330838.10:c.6973T>G	ENSP00000332265.6:p.Ser2325Ala
ENST00000358602.8:c.7726T>G	ENSP00000351416.4:p.Ser2576Ala
ENST00000509867.6:c.7387T>G	ENSP00000427151.2:p.Ser2463Ala
ENST00000558247.5:c.7377T>G
NM_001286771.1:c.7387T>G	NP_001273700.1:p.Ser2463Ala
NM_032217.3:c.7726T>G	NP_115593.3:p.Ser2576Ala
NM_198889.1:c.6973T>G	NP_942592.1:p.Ser2325Ala
XM_005265667.3:c.7723T>G	XP_005265724.1:p.Ser2575Ala
XM_005265671.3:c.6970T>G	XP_005265728.1:p.Ser2324Ala
NM_001286771.2:c.7387T>G	NP_001273700.1:p.Ser2463Ala
NM_015574.1:c.7723T>G	NP_056389.1:p.Ser2575Ala
NM_032217.4:c.7726T>G	NP_115593.3:p.Ser2576Ala
NM_198889.2:c.6973T>G	NP_942592.1:p.Ser2325Ala
XM_005265671.4:c.6970T>G	XP_005265728.1:p.Ser2324Ala
XM_017008011.1:c.7384T>G	XP_016863500.1:p.Ser2462Ala
XM_017008012.1:c.6634T>G	XP_016863501.1:p.Ser2212Ala
XM_017008013.1:c.6631T>G	XP_016863502.1:p.Ser2211Ala
NM_001286771.3:c.7387T>G	NP_001273700.1:p.Ser2463Ala
NM_015574.2:c.7723T>G	NP_056389.1:p.Ser2575Ala
NM_032217.5:c.7726T>G MANE Select	NP_115593.3:p.Ser2576Ala
NM_198889.3:c.6973T>G	NP_942592.1:p.Ser2325Ala