Canonical Allele Identifier: CA2250816624

Gene: ATPAF2

Linked Data

• dbSNP Id: rs2044408992

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18018027C>G , CM000679.2:g.18018027C>G	GRCh38
NC_000017.10:g.17921341C>G , CM000679.1:g.17921341C>G	GRCh37
NC_000017.9:g.17862066C>G	NCBI36
NG_012824.1:g.26140G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.*522G>C MANE Select	ENSP00000417190.2:n.*522G>C
ENST00000462733.5:c.*150-1767G>C	ENSP00000463920.1:n.*150-1767G>C
ENST00000474627.7:c.*522G>C	ENSP00000417190.2:n.*522G>C
ENST00000584205.5:c.*33+6597G>C	ENSP00000462899.1:n.*33+6597G>C
ENST00000585101.5:c.*34-1767G>C	ENSP00000463861.1:n.*34-1767G>C
NM_145691.3:c.*522G>C	NP_663729.1:n.*522G>C
XM_011524062.1:c.732+3096G>C	XP_011522364.1:n.732+3096G>C
XM_011524063.1:c.732+3096G>C	XP_011522365.1:n.732+3096G>C
XM_011524064.1:c.432+3096G>C	XP_011522366.1:n.432+3096G>C
XM_011524065.1:c.733-1767G>C	XP_011522367.1:n.733-1767G>C
XM_011524066.1:c.195+3096G>C	XP_011522368.1:n.195+3096G>C
XM_011524065.2:c.733-1767G>C	XP_011522367.1:n.733-1767G>C
XM_017025303.1:c.433-1767G>C	XP_016880792.1:n.433-1767G>C
XR_001752677.2:n.1789G>C
NM_145691.4:c.*522G>C MANE Select	NP_663729.1:n.*522G>C