Canonical Allele Identifier: CA398580555

Gene: ATPAF2

Linked Data

• MyVariant Identifiers: chr17:g.17942299T>C (hg19) ; chr17:g.18038985T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18038985T>C , CM000679.2:g.18038985T>C	GRCh38
NC_000017.10:g.17942299T>C , CM000679.1:g.17942299T>C	GRCh37
NC_000017.9:g.17883024T>C	NCBI36
NG_012824.1:g.5182A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.29A>G MANE Select	ENSP00000417190.2:p.Asp10Gly
ENST00000444058.1:c.29A>G	ENSP00000397198.1:p.Asp10Gly
ENST00000462733.5:c.29A>G	ENSP00000463920.1:p.Asp10Gly
ENST00000474627.7:c.29A>G	ENSP00000417190.2:p.Asp10Gly
ENST00000497871.1:n.217A>G
ENST00000577586.5:n.180A>G
ENST00000584205.5:c.29A>G	ENSP00000462899.1:p.Asp10Gly
ENST00000585101.5:c.29A>G	ENSP00000463861.1:p.Asp10Gly
NM_145691.3:c.29A>G	NP_663729.1:p.Asp10Gly
XM_005256848.2:c.29A>G	XP_005256905.1:p.Asp10Gly
XM_011524062.1:c.29A>G	XP_011522364.1:p.Asp10Gly
XM_011524063.1:c.29A>G	XP_011522365.1:p.Asp10Gly
XM_011524064.1:c.-126A>G	XP_011522366.1:n.-126A>G
XM_011524065.1:c.29A>G	XP_011522367.1:p.Asp10Gly
XR_934116.1:n.185A>G
XM_005256848.4:c.29A>G	XP_005256905.1:p.Asp10Gly
XM_011524065.2:c.29A>G	XP_011522367.1:p.Asp10Gly
XM_017025302.1:c.-126A>G	XP_016880791.1:n.-126A>G
XM_017025303.1:c.-126A>G	XP_016880792.1:n.-126A>G
XR_001752677.2:n.184A>G
NM_145691.4:c.29A>G MANE Select	NP_663729.1:p.Asp10Gly