Canonical Allele Identifier: CA498198957

Gene: ATPAF2

Linked Data

• gnomAD v4: 17-18021222-A-G
• MyVariant Identifiers: chr17:g.17924536A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18021222A>G , CM000679.2:g.18021222A>G	GRCh38
NC_000017.10:g.17924536A>G , CM000679.1:g.17924536A>G	GRCh37
NC_000017.9:g.17865261A>G	NCBI36
NG_012824.1:g.22945T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.633T>C MANE Select	ENSP00000417190.2:p.Ala211=
ENST00000462733.5:c.*50T>C	ENSP00000463920.1:n.*50T>C
ENST00000465337.2:n.492T>C
ENST00000467560.5:n.43T>C
ENST00000469327.5:n.543T>C
ENST00000474627.7:c.633T>C	ENSP00000417190.2:p.Ala211=
ENST00000488753.1:n.428T>C
ENST00000496852.5:n.1138T>C
ENST00000581698.1:c.49-2536T>C
ENST00000584205.5:c.*33+3402T>C	ENSP00000462899.1:n.*33+3402T>C
ENST00000585101.5:c.*33+3402T>C	ENSP00000463861.1:n.*33+3402T>C
NM_145691.3:c.633T>C	NP_663729.1:p.Ala211=
XM_005256848.2:c.633T>C	XP_005256905.1:p.Ala211=
XM_011524062.1:c.633T>C	XP_011522364.1:p.Ala211=
XM_011524063.1:c.633T>C	XP_011522365.1:p.Ala211=
XM_011524064.1:c.333T>C	XP_011522366.1:p.Ala111=
XM_011524065.1:c.633T>C	XP_011522367.1:p.Ala211=
XM_011524066.1:c.96T>C	XP_011522368.1:p.Ala32=
XR_934116.1:n.1031T>C
XM_005256848.4:c.633T>C	XP_005256905.1:p.Ala211=
XM_011524065.2:c.633T>C	XP_011522367.1:p.Ala211=
XM_017025302.1:c.333T>C	XP_016880791.1:p.Ala111=
XM_017025303.1:c.333T>C	XP_016880792.1:p.Ala111=
XR_001752677.2:n.1030T>C
NM_145691.4:c.633T>C MANE Select	NP_663729.1:p.Ala211=