Canonical Allele Identifier: CA498198857

Gene: ATPAF2

Linked Data

• MyVariant Identifiers: chr17:g.17924455G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18021141G>C , CM000679.2:g.18021141G>C	GRCh38
NC_000017.10:g.17924455G>C , CM000679.1:g.17924455G>C	GRCh37
NC_000017.9:g.17865180G>C	NCBI36
NG_012824.1:g.23026C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.714C>G MANE Select	ENSP00000417190.2:p.Arg238=
ENST00000462733.5:c.*131C>G	ENSP00000463920.1:n.*131C>G
ENST00000465337.2:n.573C>G
ENST00000467560.5:n.124C>G
ENST00000469327.5:n.624C>G
ENST00000474627.7:c.714C>G	ENSP00000417190.2:p.Arg238=
ENST00000488753.1:n.509C>G
ENST00000496852.5:n.1219C>G
ENST00000581698.1:c.49-2455C>G
ENST00000584205.5:c.*33+3483C>G	ENSP00000462899.1:n.*33+3483C>G
ENST00000585101.5:c.*33+3483C>G	ENSP00000463861.1:n.*33+3483C>G
NM_145691.3:c.714C>G	NP_663729.1:p.Arg238=
XM_005256848.2:c.714C>G	XP_005256905.1:p.Arg238=
XM_011524062.1:c.714C>G	XP_011522364.1:p.Arg238=
XM_011524063.1:c.714C>G	XP_011522365.1:p.Arg238=
XM_011524064.1:c.414C>G	XP_011522366.1:p.Arg138=
XM_011524065.1:c.714C>G	XP_011522367.1:p.Arg238=
XM_011524066.1:c.177C>G	XP_011522368.1:p.Arg59=
XM_005256848.4:c.714C>G	XP_005256905.1:p.Arg238=
XM_011524065.2:c.714C>G	XP_011522367.1:p.Arg238=
XM_017025302.1:c.414C>G	XP_016880791.1:p.Arg138=
XM_017025303.1:c.414C>G	XP_016880792.1:p.Arg138=
XR_001752677.2:n.1111C>G
NM_145691.4:c.714C>G MANE Select	NP_663729.1:p.Arg238=