Canonical Allele Identifier: CA498198977

Gene: ATPAF2

Linked Data

• MyVariant Identifiers: chr17:g.17924551C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18021237C>A , CM000679.2:g.18021237C>A	GRCh38
NC_000017.10:g.17924551C>A , CM000679.1:g.17924551C>A	GRCh37
NC_000017.9:g.17865276C>A	NCBI36
NG_012824.1:g.22930G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.618G>T MANE Select	ENSP00000417190.2:p.Gly206=
ENST00000462733.5:c.*35G>T	ENSP00000463920.1:n.*35G>T
ENST00000465337.2:n.477G>T
ENST00000467560.5:n.28G>T
ENST00000469327.5:n.528G>T
ENST00000474627.7:c.618G>T	ENSP00000417190.2:p.Gly206=
ENST00000488753.1:n.413G>T
ENST00000496852.5:n.1123G>T
ENST00000581698.1:c.49-2551G>T
ENST00000584205.5:c.*33+3387G>T	ENSP00000462899.1:n.*33+3387G>T
ENST00000585101.5:c.*33+3387G>T	ENSP00000463861.1:n.*33+3387G>T
NM_145691.3:c.618G>T	NP_663729.1:p.Gly206=
XM_005256848.2:c.618G>T	XP_005256905.1:p.Gly206=
XM_011524062.1:c.618G>T	XP_011522364.1:p.Gly206=
XM_011524063.1:c.618G>T	XP_011522365.1:p.Gly206=
XM_011524064.1:c.318G>T	XP_011522366.1:p.Gly106=
XM_011524065.1:c.618G>T	XP_011522367.1:p.Gly206=
XM_011524066.1:c.81G>T	XP_011522368.1:p.Gly27=
XR_934116.1:n.1016G>T
XM_005256848.4:c.618G>T	XP_005256905.1:p.Gly206=
XM_011524065.2:c.618G>T	XP_011522367.1:p.Gly206=
XM_017025302.1:c.318G>T	XP_016880791.1:p.Gly106=
XM_017025303.1:c.318G>T	XP_016880792.1:p.Gly106=
XR_001752677.2:n.1015G>T
NM_145691.4:c.618G>T MANE Select	NP_663729.1:p.Gly206=