Canonical Allele Identifier: CA2838420057

Gene: ZNF608

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.124647828dup , CM000667.2:g.124647828dup	GRCh38
NC_000005.9:g.123983521dup , CM000667.1:g.123983521dup	GRCh37
NC_000005.8:g.124011420dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513986.2:c.2561dup MANE Select	ENSP00000421899.2:p.Leu854PhefsTer9
ENST00000306315.9:c.2561dup	ENSP00000307746.5:p.Leu854PhefsTer9
ENST00000503896.6:n.628+1787dup
ENST00000504926.5:c.1280dup	ENSP00000427657.1:p.Leu427PhefsTer9
ENST00000505686.5:c.1250+1787dup	ENSP00000424086.1:n.1250+1787dup
ENST00000613878.4:c.1250+1787dup	ENSP00000477767.1:n.1250+1787dup
NM_020747.2:c.2561dup	NP_065798.2:p.Leu854PhefsTer9
XM_005272037.2:c.2561dup	XP_005272094.1:p.Leu854PhefsTer9
XM_005272038.1:c.2561dup	XP_005272095.1:p.Leu854PhefsTer9
XM_005272039.2:c.2561dup	XP_005272096.1:p.Leu854PhefsTer9
XM_005272040.2:c.1697dup	XP_005272097.1:p.Leu566PhefsTer9
XM_011543520.1:c.2561dup	XP_011541822.1:p.Leu854PhefsTer9
XM_011543521.1:c.1736dup	XP_011541823.1:p.Leu579PhefsTer9
XM_011543522.1:c.1670dup	XP_011541824.1:p.Leu557PhefsTer9
XM_011543523.1:c.1406dup	XP_011541825.1:p.Leu469PhefsTer9
XR_246536.2:n.3446dup
XM_005272037.3:c.2561dup	XP_005272094.1:p.Leu854PhefsTer9
XM_005272038.2:c.2561dup	XP_005272095.1:p.Leu854PhefsTer9
XM_005272039.3:c.2561dup	XP_005272096.1:p.Leu854PhefsTer9
XM_005272040.4:c.1697dup	XP_005272097.1:p.Leu566PhefsTer9
XM_011543520.3:c.2561dup	XP_011541822.1:p.Leu854PhefsTer9
XM_011543522.3:c.1670dup	XP_011541824.1:p.Leu557PhefsTer9
XM_011543523.2:c.1406dup	XP_011541825.1:p.Leu469PhefsTer9
XR_001742165.2:n.3170dup
XR_246536.4:n.3170dup
NM_001385619.1:c.2561dup	NP_001372548.1:p.Leu854PhefsTer9
NM_001385620.1:c.2561dup	NP_001372549.1:p.Leu854PhefsTer9
NM_001385621.1:c.1697dup	NP_001372550.1:p.Leu566PhefsTer9
NM_020747.3:c.2561dup MANE Select	NP_065798.2:p.Leu854PhefsTer9