Canonical Allele Identifier: CA325193

Gene: ATPAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18018529G>C , CM000679.2:g.18018529G>C	GRCh38
NC_000017.10:g.17921843G>C , CM000679.1:g.17921843G>C	GRCh37
NC_000017.9:g.17862568G>C	NCBI36
NG_012824.1:g.25638C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_145691.4:c.*20C>G MANE Select	NP_663729.1:n.*20C>G
ENST00000474627.8:c.*20C>G MANE Select	ENSP00000417190.2:n.*20C>G
NM_145691.3:c.*20C>G	NP_663729.1:n.*20C>G
ENST00000462733.5:c.*150-2269C>G	ENSP00000463920.1:n.*150-2269C>G
ENST00000467560.5:n.300C>G
ENST00000474627.7:c.*20C>G	ENSP00000417190.2:n.*20C>G
ENST00000496852.5:n.1395C>G
ENST00000581698.1:c.206C>G
ENST00000584205.5:c.*33+6095C>G	ENSP00000462899.1:n.*33+6095C>G
ENST00000585101.5:c.*34-2269C>G	ENSP00000463861.1:n.*34-2269C>G
XM_011524062.1:c.732+2594C>G	XP_011522364.1:n.732+2594C>G
XM_011524063.1:c.732+2594C>G	XP_011522365.1:n.732+2594C>G
XM_011524064.1:c.432+2594C>G	XP_011522366.1:n.432+2594C>G
XM_011524065.1:c.733-2269C>G	XP_011522367.1:n.733-2269C>G
XM_011524065.2:c.733-2269C>G	XP_011522367.1:n.733-2269C>G
XM_011524066.1:c.195+2594C>G	XP_011522368.1:n.195+2594C>G
XM_017025302.1:c.*20C>G	XP_016880791.1:n.*20C>G
XM_017025303.1:c.433-2269C>G	XP_016880792.1:n.433-2269C>G
XR_001752677.2:n.1287C>G