Canonical Allele Identifier: CA9886077

Gene: ZNF335

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45968325G>A , CM000682.2:g.45968325G>A	GRCh38
NC_000020.10:g.44596964G>A , CM000682.1:g.44596964G>A	GRCh37
NC_000020.9:g.44030371G>A	NCBI36
NG_029772.1:g.8870C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022095.4:c.480C>T MANE Select	NP_071378.1:p.Ala160=
ENST00000322927.3:c.480C>T MANE Select	ENSP00000325326.2:p.Ala160=
NM_022095.3:c.480C>T	NP_071378.1:p.Ala160=
ENST00000322927.2:c.480C>T	ENSP00000325326.2:p.Ala160=
ENST00000476822.1:n.813C>T
ENST00000494955.1:n.534C>T
XM_005260504.3:c.480C>T	XP_005260561.1:p.Ala160=
XM_005260504.4:c.480C>T	XP_005260561.1:p.Ala160=
XM_005260506.2:c.-49C>T	XP_005260563.1:n.-49C>T
XM_011528979.1:c.480C>T	XP_011527281.1:p.Ala160=
XM_011528979.3:c.480C>T	XP_011527281.1:p.Ala160=
XM_017028012.1:c.-49C>T	XP_016883501.1:n.-49C>T
XR_001754372.2:n.971C>T
XR_002958500.1:n.971C>T
XR_002958501.1:n.971C>T
XR_936602.1:n.991C>T
XR_936602.3:n.971C>T
XR_936603.1:n.992C>T
XR_936604.1:n.992C>T
XR_936604.3:n.971C>T