Canonical Allele Identifier: CA2250816739

Gene: ATPAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18018082A= , CM000679.2:g.18018082A=	GRCh38
NC_000017.10:g.17921396A= , CM000679.1:g.17921396A=	GRCh37
NC_000017.9:g.17862121A=	NCBI36
NG_012824.1:g.26085T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.*467T= MANE Select	ENSP00000417190.2:n.*467T=
ENST00000462733.5:c.*150-1822T=	ENSP00000463920.1:n.*150-1822T=
ENST00000474627.7:c.*467T=	ENSP00000417190.2:n.*467T=
ENST00000584205.5:c.*33+6542T=	ENSP00000462899.1:n.*33+6542T=
ENST00000585101.5:c.*34-1822T=	ENSP00000463861.1:n.*34-1822T=
NM_145691.3:c.*467T=	NP_663729.1:n.*467T=
XM_011524062.1:c.732+3041T=	XP_011522364.1:n.732+3041T=
XM_011524063.1:c.732+3041T=	XP_011522365.1:n.732+3041T=
XM_011524064.1:c.432+3041T=	XP_011522366.1:n.432+3041T=
XM_011524065.1:c.733-1822T=	XP_011522367.1:n.733-1822T=
XM_011524066.1:c.195+3041T=	XP_011522368.1:n.195+3041T=
XM_011524065.2:c.733-1822T=	XP_011522367.1:n.733-1822T=
XM_017025303.1:c.433-1822T=	XP_016880792.1:n.433-1822T=
XR_001752677.2:n.1734T=
NM_145691.4:c.*467T= MANE Select	NP_663729.1:n.*467T=