Canonical Allele Identifier: CA413065123

Gene: ZNF81

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47916544C>G , CM000685.2:g.47916544C>G	GRCh38
NC_000023.10:g.47775943C>G , CM000685.1:g.47775943C>G	GRCh37
NC_000023.9:g.47660887C>G	NCBI36
NG_021266.1:g.84643C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_007137.5:c.1898C>G MANE Select	NP_009068.2:p.Thr633Ser
ENST00000338637.13:c.1898C>G MANE Select	ENSP00000341151.7:p.Thr633Ser
NM_001378152.1:c.1898C>G	NP_001365081.1:p.Thr633Ser
NM_001378153.1:c.1898C>G	NP_001365082.1:p.Thr633Ser
NM_001378154.1:c.278-7380C>G	NP_001365083.1:n.278-7380C>G
NM_001378155.1:c.278-4764C>G	NP_001365084.1:n.278-4764C>G
NM_007137.3:c.1898C>G	NP_009068.2:p.Thr633Ser
ENST00000338637.11:c.1898C>G	ENSP00000341151.7:p.Thr633Ser
ENST00000376950.4:c.277+20604C>G	ENSP00000366149.4:n.277+20604C>G
ENST00000376954.5:c.1898C>G	ENSP00000366153.1:p.Thr633Ser
ENST00000376954.6:c.1898C>G	ENSP00000366153.1:p.Thr633Ser
XM_005272600.2:c.1898C>G	XP_005272657.1:p.Thr633Ser
XM_005272600.3:c.1898C>G	XP_005272657.1:p.Thr633Ser
XM_011543899.1:c.1898C>G	XP_011542201.1:p.Thr633Ser
XM_011543899.2:c.1898C>G	XP_011542201.1:p.Thr633Ser
XM_011543900.1:c.1898C>G	XP_011542202.1:p.Thr633Ser
XM_011543900.2:c.1898C>G	XP_011542202.1:p.Thr633Ser
XM_011543901.1:c.1898C>G	XP_011542203.1:p.Thr633Ser
XM_011543902.1:c.1898C>G	XP_011542204.1:p.Thr633Ser
XM_017029486.1:c.1898C>G	XP_016884975.1:p.Thr633Ser
XM_017029487.1:c.1898C>G	XP_016884976.1:p.Thr633Ser