Canonical Allele Identifier: CA2341584695

Gene: ZNF577

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51869633C= , CM000681.2:g.51869633C=	GRCh38
NC_000019.9:g.52372886C= , CM000681.1:g.52372886C=	GRCh37
NC_000019.8:g.57064698C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301399.12:c.*2899G=	ENSP00000301399.5:n.*2899G=
ENST00000451628.9:c.*2899G=	ENSP00000389652.2:n.*2899G=
ENST00000638348.2:c.*2899G= MANE Select	ENSP00000491936.2:n.*2899G=
ENST00000639636.2:c.*2899G=	ENSP00000491349.1:n.*2899G=
ENST00000638827.1:c.283+7649G=	ENSP00000492704.1:n.283+7649G=
ENST00000638875.1:n.220+1995G=
ENST00000639703.1:n.400+7649G=
ENST00000640678.1:n.1561+7649G=
ENST00000640955.1:n.1632+7649G=
ENST00000412216.5:c.283+7649G=	ENSP00000394828.1:n.283+7649G=
ENST00000477228.1:n.1561+7649G=
ENST00000485702.5:n.400+7649G=
ENST00000586437.5:n.220+1995G=
NR_024181.1:n.698+7649G=
NM_001370447.1:c.*2899G=	NP_001357376.1:n.*2899G=
NM_001370448.1:c.*2899G=	NP_001357377.1:n.*2899G=
NM_001370449.1:c.*2899G= MANE Select	NP_001357378.1:n.*2899G=
NM_001370450.1:c.*2899G=	NP_001357379.1:n.*2899G=
NM_001370452.1:c.283+7649G=	NP_001357381.1:n.283+7649G=
NM_001370455.1:c.283+7649G=	NP_001357384.1:n.283+7649G=
NM_001370456.1:c.283+7649G=	NP_001357385.1:n.283+7649G=
NM_001370457.1:c.283+7649G=	NP_001357386.1:n.283+7649G=
NR_163433.1:n.1632+7649G=
NM_001135590.2:c.*2899G=	NP_001129062.1:n.*2899G=
NM_032679.3:c.*2899G=	NP_116068.2:n.*2899G=