Canonical Allele Identifier: CA398574375

Gene: ATPAF2

Linked Data

• MyVariant Identifiers: chr17:g.17924535C>G (hg19) ; chr17:g.18021221C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18021221C>G , CM000679.2:g.18021221C>G	GRCh38
NC_000017.10:g.17924535C>G , CM000679.1:g.17924535C>G	GRCh37
NC_000017.9:g.17865260C>G	NCBI36
NG_012824.1:g.22946G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.634G>C MANE Select	ENSP00000417190.2:p.Ala212Pro
ENST00000462733.5:c.*51G>C	ENSP00000463920.1:n.*51G>C
ENST00000465337.2:n.493G>C
ENST00000467560.5:n.44G>C
ENST00000469327.5:n.544G>C
ENST00000474627.7:c.634G>C	ENSP00000417190.2:p.Ala212Pro
ENST00000488753.1:n.429G>C
ENST00000496852.5:n.1139G>C
ENST00000581698.1:c.49-2535G>C
ENST00000584205.5:c.*33+3403G>C	ENSP00000462899.1:n.*33+3403G>C
ENST00000585101.5:c.*33+3403G>C	ENSP00000463861.1:n.*33+3403G>C
NM_145691.3:c.634G>C	NP_663729.1:p.Ala212Pro
XM_005256848.2:c.634G>C	XP_005256905.1:p.Ala212Pro
XM_011524062.1:c.634G>C	XP_011522364.1:p.Ala212Pro
XM_011524063.1:c.634G>C	XP_011522365.1:p.Ala212Pro
XM_011524064.1:c.334G>C	XP_011522366.1:p.Ala112Pro
XM_011524065.1:c.634G>C	XP_011522367.1:p.Ala212Pro
XM_011524066.1:c.97G>C	XP_011522368.1:p.Ala33Pro
XR_934116.1:n.1032G>C
XM_005256848.4:c.634G>C	XP_005256905.1:p.Ala212Pro
XM_011524065.2:c.634G>C	XP_011522367.1:p.Ala212Pro
XM_017025302.1:c.334G>C	XP_016880791.1:p.Ala112Pro
XM_017025303.1:c.334G>C	XP_016880792.1:p.Ala112Pro
XR_001752677.2:n.1031G>C
NM_145691.4:c.634G>C MANE Select	NP_663729.1:p.Ala212Pro