Canonical Allele Identifier: CA636176207
Community Standard Title: NM_022095.4(ZNF335):c.3488-16dup
Gene: ZNF335 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45950085dup , CM000682.2:g.45950085dup GRCh38
NC_000020.10:g.44578724dup , CM000682.1:g.44578724dup GRCh37
NC_000020.9:g.44012131dup NCBI36
NG_029772.1:g.27110dup

Transcript Alleles

HGVS Amino-acid Change
NM_022095.4:c.3488-16dup MANE Select NP_071378.1:n.3488-16dup
ENST00000322927.3:c.3488-16dup MANE Select ENSP00000325326.2:n.3488-16dup
NM_022095.3:c.3488-16dup NP_071378.1:n.3488-16dup
ENST00000322927.2:c.3488-16dup ENSP00000325326.2:n.3488-16dup
XM_005260504.3:c.3485-16dup XP_005260561.1:n.3485-16dup
XM_005260504.4:c.3485-16dup XP_005260561.1:n.3485-16dup
XM_005260506.2:c.2960-16dup XP_005260563.1:n.2960-16dup
XM_017028012.1:c.2960-16dup XP_016883501.1:n.2960-16dup
XR_002958500.1:n.5435-16dup
XR_002958501.1:n.3884-16dup
XR_936602.3:n.3999-16dup