Canonical Allele Identifier: CA398580556

Gene: ATPAF2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.29A>C MANE Select	ENSP00000417190.2:p.Asp10Ala
ENST00000444058.1:c.29A>C	ENSP00000397198.1:p.Asp10Ala
ENST00000462733.5:c.29A>C	ENSP00000463920.1:p.Asp10Ala
ENST00000474627.7:c.29A>C	ENSP00000417190.2:p.Asp10Ala
ENST00000497871.1:n.217A>C
ENST00000577586.5:n.180A>C
ENST00000584205.5:c.29A>C	ENSP00000462899.1:p.Asp10Ala
ENST00000585101.5:c.29A>C	ENSP00000463861.1:p.Asp10Ala
NM_145691.3:c.29A>C	NP_663729.1:p.Asp10Ala
XM_005256848.2:c.29A>C	XP_005256905.1:p.Asp10Ala
XM_011524062.1:c.29A>C	XP_011522364.1:p.Asp10Ala
XM_011524063.1:c.29A>C	XP_011522365.1:p.Asp10Ala
XM_011524064.1:c.-126A>C	XP_011522366.1:n.-126A>C
XM_011524065.1:c.29A>C	XP_011522367.1:p.Asp10Ala
XR_934116.1:n.185A>C
XM_005256848.4:c.29A>C	XP_005256905.1:p.Asp10Ala
XM_011524065.2:c.29A>C	XP_011522367.1:p.Asp10Ala
XM_017025302.1:c.-126A>C	XP_016880791.1:n.-126A>C
XM_017025303.1:c.-126A>C	XP_016880792.1:n.-126A>C
XR_001752677.2:n.184A>C
NM_145691.4:c.29A>C MANE Select	NP_663729.1:p.Asp10Ala