Canonical Allele Identifier: CA377082706

Gene: ZNF365

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62655425C>G , CM000672.2:g.62655425C>G	GRCh38
NC_000010.10:g.64415185C>G , CM000672.1:g.64415185C>G	GRCh37
NC_000010.9:g.64085191C>G	NCBI36
NG_021209.1:g.286270C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.1130-971C>G	ENSP00000502188.1:n.1130-971C>G
ENST00000344640.7:c.126+495C>G	ENSP00000345300.3:n.126+495C>G
ENST00000373784.6:c.126+495C>G	ENSP00000362889.2:n.126+495C>G
ENST00000395249.5:c.39-10704C>G	ENSP00000378670.1:n.39-10704C>G
ENST00000395251.5:c.185C>G	ENSP00000378672.1:p.Thr62Ser
ENST00000410046.7:c.1130-971C>G	ENSP00000387091.3:n.1130-971C>G
ENST00000461412.1:n.240C>G
ENST00000614806.1:c.185C>G	ENSP00000481372.1:p.Thr62Ser
NM_199451.2:c.1130-971C>G	NP_955523.1:n.1130-971C>G
NM_199452.3:c.185C>G	NP_955524.3:p.Ala62Gly
XM_011539530.1:c.341C>G	XP_011537832.1:p.Thr114Ser
XM_011539531.1:c.341C>G	XP_011537833.1:p.Thr114Ser
XM_011539532.1:c.185C>G	XP_011537834.1:p.Thr62Ser
XM_011539533.1:c.341C>G	XP_011537835.1:p.Thr114Ser
XR_946002.1:n.81+1G>C
XM_017015938.1:c.341C>G	XP_016871427.1:p.Thr114Ser
XM_017015939.1:c.341C>G	XP_016871428.1:p.Thr114Ser
XM_017015940.1:c.185C>G	XP_016871429.1:p.Thr62Ser
XM_017015941.1:c.341C>G	XP_016871430.1:p.Thr114Ser
XR_946002.2:n.81+1G>C
NM_199451.3:c.1130-971C>G	NP_955523.1:n.1130-971C>G