Canonical Allele Identifier: CA498199382

Gene: ATPAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18024647T>G , CM000679.2:g.18024647T>G	GRCh38
NC_000017.10:g.17927961T>G , CM000679.1:g.17927961T>G	GRCh37
NC_000017.9:g.17868686T>G	NCBI36
NG_012824.1:g.19520A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_145691.4:c.480A>C MANE Select	NP_663729.1:p.Pro160=
ENST00000474627.8:c.480A>C MANE Select	ENSP00000417190.2:p.Pro160=
NM_145691.3:c.480A>C	NP_663729.1:p.Pro160=
ENST00000444058.1:c.480A>C	ENSP00000397198.1:p.Pro160=
ENST00000462733.5:c.*10A>C	ENSP00000463920.1:n.*10A>C
ENST00000469327.5:n.148A>C
ENST00000474627.7:c.480A>C	ENSP00000417190.2:p.Pro160=
ENST00000488753.1:n.275A>C
ENST00000496852.5:n.985A>C
ENST00000581698.1:c.25A>C
ENST00000584205.5:c.*10A>C	ENSP00000462899.1:n.*10A>C
ENST00000585101.5:c.*10A>C	ENSP00000463861.1:n.*10A>C
XM_005256848.2:c.480A>C	XP_005256905.1:p.Pro160=
XM_005256848.4:c.480A>C	XP_005256905.1:p.Pro160=
XM_011524062.1:c.480A>C	XP_011522364.1:p.Pro160=
XM_011524063.1:c.480A>C	XP_011522365.1:p.Pro160=
XM_011524064.1:c.180A>C	XP_011522366.1:p.Pro60=
XM_011524065.1:c.480A>C	XP_011522367.1:p.Pro160=
XM_011524065.2:c.480A>C	XP_011522367.1:p.Pro160=
XM_011524066.1:c.-58A>C	XP_011522368.1:n.-58A>C
XM_017025302.1:c.180A>C	XP_016880791.1:p.Pro60=
XM_017025303.1:c.180A>C	XP_016880792.1:p.Pro60=
XR_001752677.2:n.635A>C
XR_934116.1:n.636A>C