Canonical Allele Identifier: CA2342022595

Gene: ZNF600

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52780732_52780740delinsAAAACAAAC , CM000681.2:g.52780732_52780740delinsAAAACAAAC	GRCh38
NC_000019.9:g.53283985_53283993delinsAAAACAAAC , CM000681.1:g.53283985_53283993delinsAAAACAAAC	GRCh37
NC_000019.8:g.57975797_57975805delinsAAAACAAAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685388.1:c.-19-1833_-19-1825delinsGTTTGTTTT	ENSP00000510246.1:n.-19-1833_-19-1825delinsGTTTGTTTT
ENST00000688329.1:c.-162-17_-162-9delinsGTTTGTTTT	ENSP00000509375.1:n.-162-17_-162-9delinsGTTTGTTTT
ENST00000692063.1:c.-179_-171delinsGTTTGTTTT MANE Select	ENSP00000509267.1:n.-179_-171delinsGTTTGTTTT
ENST00000647907.1:c.-19-1833_-19-1825delinsGTTTGTTTT	ENSP00000497989.1:n.-19-1833_-19-1825delinsGTTTGTTTT
ENST00000648893.1:c.-20+577_-20+585delinsGTTTGTTTT	ENSP00000497895.1:n.-20+577_-20+585delinsGTTTGTTTT
ENST00000648973.1:c.-19-1833_-19-1825delinsGTTTGTTTT	ENSP00000497540.1:n.-19-1833_-19-1825delinsGTTTGTTTT
ENST00000338230.3:c.-99-1833_-99-1825delinsGTTTGTTTT	ENSP00000344791.2:n.-99-1833_-99-1825delinsGTTTGTTTT
ENST00000360272.5:c.824-13727_824-13719delinsGTTTGTTTT	ENSP00000353410.5:n.824-13727_824-13719delinsGTTTGTTTT
ENST00000599893.1:n.513_521delinsGTTTGTTTT
NM_198457.2:c.-99-1833_-99-1825delinsGTTTGTTTT	NP_940859.2:n.-99-1833_-99-1825delinsGTTTGTTTT
XM_005258576.3:c.-19-1833_-19-1825delinsGTTTGTTTT	XP_005258633.1:n.-19-1833_-19-1825delinsGTTTGTTTT
XM_006723055.2:c.-19-1833_-19-1825delinsGTTTGTTTT	XP_006723118.1:n.-19-1833_-19-1825delinsGTTTGTTTT
XM_006723057.2:c.64-6039_64-6031delinsGTTTGTTTT	XP_006723120.1:n.64-6039_64-6031delinsGTTTGTTTT
XM_006723058.2:c.64-6039_64-6031delinsGTTTGTTTT	XP_006723121.1:n.64-6039_64-6031delinsGTTTGTTTT
XM_011526563.1:c.-179_-171delinsGTTTGTTTT	XP_011524865.1:n.-179_-171delinsGTTTGTTTT
XM_011526564.1:c.-20+577_-20+585delinsGTTTGTTTT	XP_011524866.1:n.-20+577_-20+585delinsGTTTGTTTT
XM_011526565.1:c.-20+577_-20+585delinsGTTTGTTTT	XP_011524867.1:n.-20+577_-20+585delinsGTTTGTTTT
XM_011526566.1:c.-259_-251delinsGTTTGTTTT	XP_011524868.1:n.-259_-251delinsGTTTGTTTT
NM_001321866.1:c.-179_-171delinsGTTTGTTTT	NP_001308795.1:n.-179_-171delinsGTTTGTTTT
NM_001321867.1:c.-19-1833_-19-1825delinsGTTTGTTTT	NP_001308796.1:n.-19-1833_-19-1825delinsGTTTGTTTT
NM_198457.3:c.-99-1833_-99-1825delinsGTTTGTTTT	NP_940859.3:n.-99-1833_-99-1825delinsGTTTGTTTT
XM_017026390.1:c.-162-17_-162-9delinsGTTTGTTTT	XP_016881879.1:n.-162-17_-162-9delinsGTTTGTTTT
XM_017026391.1:c.-179_-171delinsGTTTGTTTT	XP_016881880.1:n.-179_-171delinsGTTTGTTTT
XM_017026392.1:c.-162-17_-162-9delinsGTTTGTTTT	XP_016881881.1:n.-162-17_-162-9delinsGTTTGTTTT
NM_001321866.2:c.-179_-171delinsGTTTGTTTT	NP_001308795.1:n.-179_-171delinsGTTTGTTTT
NM_001321867.2:c.-19-1833_-19-1825delinsGTTTGTTTT	NP_001308796.1:n.-19-1833_-19-1825delinsGTTTGTTTT
NM_198457.4:c.-99-1833_-99-1825delinsGTTTGTTTT	NP_940859.3:n.-99-1833_-99-1825delinsGTTTGTTTT
NM_001321866.3:c.-179_-171delinsGTTTGTTTT	NP_001308795.1:n.-179_-171delinsGTTTGTTTT
NM_001321867.3:c.-19-1833_-19-1825delinsGTTTGTTTT	NP_001308796.1:n.-19-1833_-19-1825delinsGTTTGTTTT
NM_198457.5:c.-99-1833_-99-1825delinsGTTTGTTTT	NP_940859.3:n.-99-1833_-99-1825delinsGTTTGTTTT
NM_001321866.4:c.-179_-171delinsGTTTGTTTT MANE Select	NP_001308795.1:n.-179_-171delinsGTTTGTTTT