Canonical Allele Identifier: CA9885766

Gene: ZNF335

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45963725C>T , CM000682.2:g.45963725C>T	GRCh38
NC_000020.10:g.44592364C>T , CM000682.1:g.44592364C>T	GRCh37
NC_000020.9:g.44025771C>T	NCBI36
NG_029772.1:g.13470G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022095.4:c.1355+13G>A MANE Select	NP_071378.1:n.1355+13G>A
ENST00000322927.3:c.1355+13G>A MANE Select	ENSP00000325326.2:n.1355+13G>A
NM_022095.3:c.1355+13G>A	NP_071378.1:n.1355+13G>A
ENST00000322927.2:c.1355+13G>A	ENSP00000325326.2:n.1355+13G>A
ENST00000475002.1:n.792G>A
XM_005260504.3:c.1352+13G>A	XP_005260561.1:n.1352+13G>A
XM_005260504.4:c.1352+13G>A	XP_005260561.1:n.1352+13G>A
XM_005260506.2:c.827+13G>A	XP_005260563.1:n.827+13G>A
XM_011528979.1:c.1355+13G>A	XP_011527281.1:n.1355+13G>A
XM_011528979.3:c.1355+13G>A	XP_011527281.1:n.1355+13G>A
XM_017028012.1:c.827+13G>A	XP_016883501.1:n.827+13G>A
XR_001754372.2:n.1846+13G>A
XR_002958500.1:n.1846+13G>A
XR_002958501.1:n.1846+13G>A
XR_936602.1:n.1866+13G>A
XR_936602.3:n.1846+13G>A
XR_936603.1:n.1867+13G>A
XR_936604.1:n.1867+13G>A
XR_936604.3:n.1846+13G>A