Canonical Allele Identifier: CA2342022652

Gene: ZNF600

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52780877T= , CM000681.2:g.52780877T=	GRCh38
NC_000019.9:g.53284130T= , CM000681.1:g.53284130T=	GRCh37
NC_000019.8:g.57975942T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685388.1:c.-19-1970A=	ENSP00000510246.1:n.-19-1970A=
ENST00000688329.1:c.-209A=	ENSP00000509375.1:n.-209A=
ENST00000692063.1:c.-316A= MANE Select	ENSP00000509267.1:n.-316A=
ENST00000647907.1:c.-19-1970A=	ENSP00000497989.1:n.-19-1970A=
ENST00000648893.1:c.-20+440A=	ENSP00000497895.1:n.-20+440A=
ENST00000648973.1:c.-19-1970A=	ENSP00000497540.1:n.-19-1970A=
ENST00000338230.3:c.-99-1970A=	ENSP00000344791.2:n.-99-1970A=
ENST00000360272.5:c.824-13864A=	ENSP00000353410.5:n.824-13864A=
ENST00000594028.1:n.457A=
ENST00000597124.1:n.285A=
ENST00000599893.1:n.376A=
NM_198457.2:c.-99-1970A=	NP_940859.2:n.-99-1970A=
XM_005258576.3:c.-19-1970A=	XP_005258633.1:n.-19-1970A=
XM_006723055.2:c.-19-1970A=	XP_006723118.1:n.-19-1970A=
XM_006723057.2:c.64-6176A=	XP_006723120.1:n.64-6176A=
XM_006723058.2:c.64-6176A=	XP_006723121.1:n.64-6176A=
XM_011526563.1:c.-316A=	XP_011524865.1:n.-316A=
XM_011526564.1:c.-20+440A=	XP_011524866.1:n.-20+440A=
XM_011526565.1:c.-20+440A=	XP_011524867.1:n.-20+440A=
XM_011526566.1:c.-396A=	XP_011524868.1:n.-396A=
NM_001321866.1:c.-316A=	NP_001308795.1:n.-316A=
NM_001321867.1:c.-19-1970A=	NP_001308796.1:n.-19-1970A=
NM_198457.3:c.-99-1970A=	NP_940859.3:n.-99-1970A=
XM_017026390.1:c.-209A=	XP_016881879.1:n.-209A=
XM_017026391.1:c.-316A=	XP_016881880.1:n.-316A=
XM_017026392.1:c.-209A=	XP_016881881.1:n.-209A=
NM_001321866.2:c.-316A=	NP_001308795.1:n.-316A=
NM_001321867.2:c.-19-1970A=	NP_001308796.1:n.-19-1970A=
NM_198457.4:c.-99-1970A=	NP_940859.3:n.-99-1970A=
NM_001321866.3:c.-316A=	NP_001308795.1:n.-316A=
NM_001321867.3:c.-19-1970A=	NP_001308796.1:n.-19-1970A=
NM_198457.5:c.-99-1970A=	NP_940859.3:n.-99-1970A=
NM_001321866.4:c.-316A= MANE Select	NP_001308795.1:n.-316A=