Canonical Allele Identifier: CA2636423901
Gene: ATPAF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18018130C>A , CM000679.2:g.18018130C>A GRCh38
NC_000017.10:g.17921444C>A , CM000679.1:g.17921444C>A GRCh37
NC_000017.9:g.17862169C>A NCBI36
NG_012824.1:g.26037G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000474627.8:c.*419G>T MANE Select ENSP00000417190.2:n.*419G>T
ENST00000462733.5:c.*150-1870G>T ENSP00000463920.1:n.*150-1870G>T
ENST00000474627.7:c.*419G>T ENSP00000417190.2:n.*419G>T
ENST00000584205.5:c.*33+6494G>T ENSP00000462899.1:n.*33+6494G>T
ENST00000585101.5:c.*34-1870G>T ENSP00000463861.1:n.*34-1870G>T
NM_145691.3:c.*419G>T NP_663729.1:n.*419G>T
XM_011524062.1:c.732+2993G>T XP_011522364.1:n.732+2993G>T
XM_011524063.1:c.732+2993G>T XP_011522365.1:n.732+2993G>T
XM_011524064.1:c.432+2993G>T XP_011522366.1:n.432+2993G>T
XM_011524065.1:c.733-1870G>T XP_011522367.1:n.733-1870G>T
XM_011524066.1:c.195+2993G>T XP_011522368.1:n.195+2993G>T
XM_011524065.2:c.733-1870G>T XP_011522367.1:n.733-1870G>T
XM_017025303.1:c.433-1870G>T XP_016880792.1:n.433-1870G>T
XR_001752677.2:n.1686G>T
NM_145691.4:c.*419G>T MANE Select NP_663729.1:n.*419G>T