Canonical Allele Identifier: CA10648738

Gene: ATPAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18039014C>A , CM000679.2:g.18039014C>A	GRCh38
NC_000017.10:g.17942328C>A , CM000679.1:g.17942328C>A	GRCh37
NC_000017.9:g.17883053C>A	NCBI36
NG_012824.1:g.5153G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_145691.4:c.-1G>T MANE Select	NP_663729.1:n.-1G>T
ENST00000474627.8:c.-1G>T MANE Select	ENSP00000417190.2:n.-1G>T
NM_145691.3:c.-1G>T	NP_663729.1:n.-1G>T
ENST00000444058.1:c.-1G>T	ENSP00000397198.1:n.-1G>T
ENST00000462733.5:c.-1G>T	ENSP00000463920.1:n.-1G>T
ENST00000474627.7:c.-1G>T	ENSP00000417190.2:n.-1G>T
ENST00000497871.1:n.188G>T
ENST00000577586.5:n.151G>T
ENST00000584205.5:c.-1G>T	ENSP00000462899.1:n.-1G>T
ENST00000585101.5:c.-1G>T	ENSP00000463861.1:n.-1G>T
XM_005256848.2:c.-1G>T	XP_005256905.1:n.-1G>T
XM_005256848.4:c.-1G>T	XP_005256905.1:n.-1G>T
XM_011524062.1:c.-1G>T	XP_011522364.1:n.-1G>T
XM_011524063.1:c.-1G>T	XP_011522365.1:n.-1G>T
XM_011524064.1:c.-155G>T	XP_011522366.1:n.-155G>T
XM_011524065.1:c.-1G>T	XP_011522367.1:n.-1G>T
XM_011524065.2:c.-1G>T	XP_011522367.1:n.-1G>T
XM_017025302.1:c.-155G>T	XP_016880791.1:n.-155G>T
XM_017025303.1:c.-155G>T	XP_016880792.1:n.-155G>T
XR_001752677.2:n.155G>T
XR_934116.1:n.156G>T