Canonical Allele Identifier: CA2636423834

Gene: ATPAF2

Linked Data

• gnomAD v4: 17-18018055-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18018055A>C , CM000679.2:g.18018055A>C	GRCh38
NC_000017.10:g.17921369A>C , CM000679.1:g.17921369A>C	GRCh37
NC_000017.9:g.17862094A>C	NCBI36
NG_012824.1:g.26112T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.*494T>G MANE Select	ENSP00000417190.2:n.*494T>G
ENST00000462733.5:c.*150-1795T>G	ENSP00000463920.1:n.*150-1795T>G
ENST00000474627.7:c.*494T>G	ENSP00000417190.2:n.*494T>G
ENST00000584205.5:c.*33+6569T>G	ENSP00000462899.1:n.*33+6569T>G
ENST00000585101.5:c.*34-1795T>G	ENSP00000463861.1:n.*34-1795T>G
NM_145691.3:c.*494T>G	NP_663729.1:n.*494T>G
XM_011524062.1:c.732+3068T>G	XP_011522364.1:n.732+3068T>G
XM_011524063.1:c.732+3068T>G	XP_011522365.1:n.732+3068T>G
XM_011524064.1:c.432+3068T>G	XP_011522366.1:n.432+3068T>G
XM_011524065.1:c.733-1795T>G	XP_011522367.1:n.733-1795T>G
XM_011524066.1:c.195+3068T>G	XP_011522368.1:n.195+3068T>G
XM_011524065.2:c.733-1795T>G	XP_011522367.1:n.733-1795T>G
XM_017025303.1:c.433-1795T>G	XP_016880792.1:n.433-1795T>G
XR_001752677.2:n.1761T>G
NM_145691.4:c.*494T>G MANE Select	NP_663729.1:n.*494T>G