Canonical Allele Identifier: CA115777

Gene: ZNF365

Linked Data

• MyVariant Identifiers: chr10:g.64415184A>A (hg19) ; chr10:g.62655424A>A (hg38)
• PubMed: PMID:12740763

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62655424A= , CM000672.2:g.62655424A=	GRCh38
NC_000010.10:g.64415184A= , CM000672.1:g.64415184A=	GRCh37
NC_000010.9:g.64085190A=	NCBI36
NG_021209.1:g.286269A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647733.1:c.1130-972A=	ENSP00000502188.1:n.1130-972A=
ENST00000344640.7:c.126+494A=	ENSP00000345300.3:n.126+494A=
ENST00000373784.6:c.126+494A=	ENSP00000362889.2:n.126+494A=
ENST00000395249.5:c.39-10705A=	ENSP00000378670.1:n.39-10705A=
ENST00000395251.5:c.184A=	ENSP00000378672.1:p.Thr62=
ENST00000410046.7:c.1130-972A=	ENSP00000387091.3:n.1130-972A=
ENST00000461412.1:n.239A=
ENST00000614806.1:c.184A=	ENSP00000481372.1:p.Thr62=
NM_199451.2:c.1130-972A=	NP_955523.1:n.1130-972A=
XM_011539530.1:c.340A=	XP_011537832.1:p.Thr114=
XM_011539531.1:c.340A=	XP_011537833.1:p.Thr114=
XM_011539532.1:c.184A=	XP_011537834.1:p.Thr62=
XM_011539533.1:c.340A=	XP_011537835.1:p.Thr114=
XR_946002.1:n.81+2T=
XM_017015938.1:c.340A=	XP_016871427.1:p.Thr114=
XM_017015939.1:c.340A=	XP_016871428.1:p.Thr114=
XM_017015940.1:c.184A=	XP_016871429.1:p.Thr62=
XM_017015941.1:c.340A=	XP_016871430.1:p.Thr114=
XR_946002.2:n.81+2T=
NM_199451.3:c.1130-972A=	NP_955523.1:n.1130-972A=