Canonical Allele Identifier: CA498198970

Gene: ATPAF2

Linked Data

• MyVariant Identifiers: chr17:g.17924542A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18021228A>G , CM000679.2:g.18021228A>G	GRCh38
NC_000017.10:g.17924542A>G , CM000679.1:g.17924542A>G	GRCh37
NC_000017.9:g.17865267A>G	NCBI36
NG_012824.1:g.22939T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.627T>C MANE Select	ENSP00000417190.2:p.Phe209=
ENST00000462733.5:c.*44T>C	ENSP00000463920.1:n.*44T>C
ENST00000465337.2:n.486T>C
ENST00000467560.5:n.37T>C
ENST00000469327.5:n.537T>C
ENST00000474627.7:c.627T>C	ENSP00000417190.2:p.Phe209=
ENST00000488753.1:n.422T>C
ENST00000496852.5:n.1132T>C
ENST00000581698.1:c.49-2542T>C
ENST00000584205.5:c.*33+3396T>C	ENSP00000462899.1:n.*33+3396T>C
ENST00000585101.5:c.*33+3396T>C	ENSP00000463861.1:n.*33+3396T>C
NM_145691.3:c.627T>C	NP_663729.1:p.Phe209=
XM_005256848.2:c.627T>C	XP_005256905.1:p.Phe209=
XM_011524062.1:c.627T>C	XP_011522364.1:p.Phe209=
XM_011524063.1:c.627T>C	XP_011522365.1:p.Phe209=
XM_011524064.1:c.327T>C	XP_011522366.1:p.Phe109=
XM_011524065.1:c.627T>C	XP_011522367.1:p.Phe209=
XM_011524066.1:c.90T>C	XP_011522368.1:p.Phe30=
XR_934116.1:n.1025T>C
XM_005256848.4:c.627T>C	XP_005256905.1:p.Phe209=
XM_011524065.2:c.627T>C	XP_011522367.1:p.Phe209=
XM_017025302.1:c.327T>C	XP_016880791.1:p.Phe109=
XM_017025303.1:c.327T>C	XP_016880792.1:p.Phe109=
XR_001752677.2:n.1024T>C
NM_145691.4:c.627T>C MANE Select	NP_663729.1:p.Phe209=