Canonical Allele Identifier: CA2341591805

Gene: ZNF577 ZNF613

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51885336T= , CM000681.2:g.51885336T=	GRCh38
NC_000019.9:g.52388589T= , CM000681.1:g.52388589T=	GRCh37
NC_000019.8:g.57080401T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000301399.12:c.-219+1485A= (ZNF577)	ENSP00000301399.5:n.-219+1485A=
ENST00000451628.9:c.-219+1485A= (ZNF577)	ENSP00000389652.2:n.-219+1485A=
ENST00000638348.2:c.-219+1485A= (ZNF577) MANE Select	ENSP00000491936.2:n.-219+1485A=
ENST00000639636.2:c.-219+1485A= (ZNF577)	ENSP00000491349.1:n.-219+1485A=
ENST00000301399.11:c.-219+1485A= (ZNF577)	ENSP00000301399.5:n.-219+1485A=
ENST00000451628.8:c.-219+1485A= (ZNF577)	ENSP00000389652.2:n.-219+1485A=
ENST00000638325.1:c.-218-4459A= (ZNF577)	ENSP00000492661.1:n.-218-4459A=
ENST00000638348.1:c.-219+1485A= (ZNF577)	ENSP00000491936.1:n.-219+1485A=
ENST00000638423.1:c.-207+1485A= (ZNF577)	ENSP00000491339.1:n.-207+1485A=
ENST00000638538.1:c.-219+780A= (ZNF577)	ENSP00000492518.1:n.-219+780A=
ENST00000638684.1:n.274+1485A= (ZNF577)
ENST00000638721.1:n.396+1485A= (ZNF577)
ENST00000638814.1:c.-219+2560A= (ZNF577)	ENSP00000492882.1:n.-219+2560A=
ENST00000638827.1:c.-219+2560A= (ZNF577)	ENSP00000492704.1:n.-219+2560A=
ENST00000639183.1:n.350+780A= (ZNF577)
ENST00000639636.1:c.-219+1485A= (ZNF577)	ENSP00000491349.1:n.-219+1485A=
ENST00000639703.1:n.177+1485A= (ZNF577)
ENST00000640429.1:c.-219+1485A= (ZNF577)	ENSP00000491381.1:n.-219+1485A=
ENST00000640955.1:n.1131+1485A= (ZNF577)
ENST00000301399.9:c.-219+1485A= (ZNF577)	ENSP00000301399.5:n.-219+1485A=
ENST00000412216.5:c.-219+1485A= (ZNF577)	ENSP00000394828.1:n.-219+1485A=
ENST00000419138.5:c.-207+1485A= (ZNF577)	ENSP00000407476.1:n.-207+1485A=
ENST00000420592.5:c.-219+1485A= (ZNF577)	ENSP00000413476.1:n.-219+1485A=
ENST00000446514.5:c.-219+780A= (ZNF577)	ENSP00000415307.1:n.-219+780A=
ENST00000451628.6:c.-219+1485A= (ZNF577)	ENSP00000389652.2:n.-219+1485A=
ENST00000453272.5:c.-218-4459A= (ZNF577)	ENSP00000413560.1:n.-218-4459A=
ENST00000458390.5:c.-219+1485A= (ZNF577)	ENSP00000404509.1:n.-219+1485A=
ENST00000484095.1:n.350+780A= (ZNF577)
ENST00000485702.5:n.177+1485A= (ZNF577)
ENST00000588878.5:n.274+1485A= (ZNF577)
ENST00000589784.1:n.396+1485A= (ZNF577)
ENST00000591320.5:c.-219+1485A= (ZNF577)	ENSP00000467575.1:n.-219+1485A=
ENST00000592321.5:c.-219+2560A= (ZNF577)	ENSP00000467321.1:n.-219+2560A=
ENST00000613007.4:c.-199+5436T= (ZNF613)	ENSP00000478924.1:n.-199+5436T=
NM_001135590.1:c.-219+1485A= (ZNF577)	NP_001129062.1:n.-219+1485A=
NM_032679.2:c.-219+1485A= (ZNF577)	NP_116068.2:n.-219+1485A=
NR_024181.1:n.197+1485A= (ZNF577)
XM_006723432.2:c.-219+1485A= (ZNF577)	XP_006723495.1:n.-219+1485A=
XM_006723433.1:c.-219+1485A= (ZNF577)	XP_006723496.1:n.-219+1485A=
XM_006723434.2:c.-219+2560A= (ZNF577)	XP_006723497.1:n.-219+2560A=
XM_011527408.1:c.-219+1485A= (ZNF577)	XP_011525710.1:n.-219+1485A=
XM_011527409.1:c.-218-4459A= (ZNF577)	XP_011525711.1:n.-218-4459A=
XM_011527412.1:c.-219+780A= (ZNF577)	XP_011525714.1:n.-219+780A=
XM_006723432.3:c.-219+1485A= (ZNF577)	XP_006723495.1:n.-219+1485A=
XM_006723433.2:c.-219+1485A= (ZNF577)	XP_006723496.1:n.-219+1485A=
XM_011527408.3:c.-219+1485A= (ZNF577)	XP_011525710.1:n.-219+1485A=
XM_017027387.2:c.-219+1485A= (ZNF577)	XP_016882876.1:n.-219+1485A=
NM_001370447.1:c.-219+1485A= (ZNF577)	NP_001357376.1:n.-219+1485A=
NM_001370448.1:c.-219+1485A= (ZNF577)	NP_001357377.1:n.-219+1485A=
NM_001370449.1:c.-219+1485A= (ZNF577) MANE Select	NP_001357378.1:n.-219+1485A=
NM_001370450.1:c.-219+1485A= (ZNF577)	NP_001357379.1:n.-219+1485A=
NM_001370452.1:c.-219+1485A= (ZNF577)	NP_001357381.1:n.-219+1485A=
NM_001370455.1:c.-219+1485A= (ZNF577)	NP_001357384.1:n.-219+1485A=
NM_001370456.1:c.-219+1485A= (ZNF577)	NP_001357385.1:n.-219+1485A=
NM_001370457.1:c.-219+1485A= (ZNF577)	NP_001357386.1:n.-219+1485A=
NR_163433.1:n.1131+1485A= (ZNF577)
NM_001135590.2:c.-219+1485A= (ZNF577)	NP_001129062.1:n.-219+1485A=
NM_032679.3:c.-219+1485A= (ZNF577)	NP_116068.2:n.-219+1485A=