Canonical Allele Identifier: CA2314984254

Gene: ZNF516

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.76389900C= , CM000680.2:g.76389900C=	GRCh38
NC_000018.9:g.74101856C= , CM000680.1:g.74101856C=	GRCh37
NC_000018.8:g.72230844C=	NCBI36
NG_032949.1:g.110291G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443185.7:c.1811-9597G= MANE Select	ENSP00000394757.2:n.1811-9597G=
ENST00000443185.6:c.1811-9597G=	ENSP00000394757.2:n.1811-9597G=
NM_014643.3:c.1811-9597G=	NP_055458.1:n.1811-9597G=
XM_011526269.1:c.1811-9597G=	XP_011524571.1:n.1811-9597G=
XM_011526270.1:c.1811-9597G=	XP_011524572.1:n.1811-9597G=
XM_011526271.1:c.1811-9597G=	XP_011524573.1:n.1811-9597G=
XM_011526272.1:c.1811-9597G=	XP_011524574.1:n.1811-9597G=
XM_011526273.1:c.1811-9597G=	XP_011524575.1:n.1811-9597G=
XM_011526274.1:c.1811-9597G=	XP_011524576.1:n.1811-9597G=
XM_011526275.1:c.1811-9597G=	XP_011524577.1:n.1811-9597G=
XM_011526276.1:c.1811-9597G=	XP_011524578.1:n.1811-9597G=
XM_011526277.1:c.1811-9597G=	XP_011524579.1:n.1811-9597G=
XR_935268.1:n.2067-9597G=
XM_011526269.2:c.1811-9597G=	XP_011524571.1:n.1811-9597G=
XM_011526270.3:c.1811-9597G=	XP_011524572.1:n.1811-9597G=
XM_011526271.3:c.1811-9597G=	XP_011524573.1:n.1811-9597G=
XM_011526273.3:c.1811-9597G=	XP_011524575.1:n.1811-9597G=
XM_011526274.3:c.1811-9597G=	XP_011524576.1:n.1811-9597G=
XM_011526275.2:c.1811-9597G=	XP_011524577.1:n.1811-9597G=
XM_011526276.2:c.1811-9597G=	XP_011524578.1:n.1811-9597G=
XM_011526277.2:c.1811-9597G=	XP_011524579.1:n.1811-9597G=
XM_017026097.2:c.1811-9597G=	XP_016881586.1:n.1811-9597G=
XR_935268.2:n.2067-9597G=
NM_014643.4:c.1811-9597G= MANE Select	NP_055458.1:n.1811-9597G=