Canonical Allele Identifier: CA395568906

Gene: ZNF747

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30534264C>A , CM000678.2:g.30534264C>A	GRCh38
NC_000016.9:g.30545585C>A , CM000678.1:g.30545585C>A	GRCh37
NC_000016.8:g.30453086C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001305018.2:c.276G>T MANE Select	NP_001291947.1:p.Lys92Asn
ENST00000693075.1:c.276G>T MANE Select	ENSP00000509633.1:p.Lys92Asn
NM_001305018.1:c.276G>T	NP_001291947.1:p.Lys92Asn
NM_001305019.1:c.276G>T	NP_001291948.1:p.Lys92Asn
NM_001305019.2:c.276G>T	NP_001291948.1:p.Lys92Asn
NM_001305020.1:c.416G>T	NP_001291949.1:p.Arg139Met
NM_001305020.2:c.416G>T	NP_001291949.1:p.Arg139Met
NM_023931.3:c.416G>T	NP_076420.1:p.Arg139Met
NM_023931.4:c.416G>T	NP_076420.1:p.Arg139Met
ENST00000252799.3:c.416G>T	ENSP00000252799.3:p.Arg139Met
ENST00000395094.3:c.416G>T	ENSP00000378528.3:p.Arg139Met
ENST00000568028.1:c.276G>T	ENSP00000457274.1:p.Lys92Asn
ENST00000568114.1:c.243G>T	ENSP00000455659.1:p.Lys81Asn
ENST00000569360.1:c.276G>T	ENSP00000454241.1:p.Lys92Asn