Canonical Allele Identifier: CA357202748

Gene: ANKRD17

Linked Data

• dbSNP Id: rs2110079549
• gnomAD v3: 4-73076974-A-T
• gnomAD v4: 4-73076974-A-T
• MyVariant Identifiers: chr4:g.73942691A>T (hg19) ; chr4:g.73076974A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000358602.9:c.7718T>A MANE Select	ENSP00000351416.4:p.Val2573Asp
ENST00000330838.10:c.6965T>A	ENSP00000332265.6:p.Val2322Asp
ENST00000358602.8:c.7718T>A	ENSP00000351416.4:p.Val2573Asp
ENST00000509867.6:c.7379T>A	ENSP00000427151.2:p.Val2460Asp
ENST00000558247.5:c.7369T>A
NM_001286771.1:c.7379T>A	NP_001273700.1:p.Val2460Asp
NM_032217.3:c.7718T>A	NP_115593.3:p.Val2573Asp
NM_198889.1:c.6965T>A	NP_942592.1:p.Val2322Asp
XM_005265667.3:c.7715T>A	XP_005265724.1:p.Val2572Asp
XM_005265671.3:c.6962T>A	XP_005265728.1:p.Val2321Asp
NM_001286771.2:c.7379T>A	NP_001273700.1:p.Val2460Asp
NM_015574.1:c.7715T>A	NP_056389.1:p.Val2572Asp
NM_032217.4:c.7718T>A	NP_115593.3:p.Val2573Asp
NM_198889.2:c.6965T>A	NP_942592.1:p.Val2322Asp
XM_005265671.4:c.6962T>A	XP_005265728.1:p.Val2321Asp
XM_017008011.1:c.7376T>A	XP_016863500.1:p.Val2459Asp
XM_017008012.1:c.6626T>A	XP_016863501.1:p.Val2209Asp
XM_017008013.1:c.6623T>A	XP_016863502.1:p.Val2208Asp
NM_001286771.3:c.7379T>A	NP_001273700.1:p.Val2460Asp
NM_015574.2:c.7715T>A	NP_056389.1:p.Val2572Asp
NM_032217.5:c.7718T>A MANE Select	NP_115593.3:p.Val2573Asp
NM_198889.3:c.6965T>A	NP_942592.1:p.Val2322Asp