Canonical Allele Identifier: CA358018
Gene: ZNF335 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45950453C>A , CM000682.2:g.45950453C>A GRCh38
NC_000020.10:g.44579092C>A , CM000682.1:g.44579092C>A GRCh37
NC_000020.9:g.44012499C>A NCBI36
NG_029772.1:g.26742G>T

Transcript Alleles

HGVS Amino-acid Change
NM_022095.4:c.3332G>T MANE Select NP_071378.1:p.Arg1111Leu
ENST00000322927.3:c.3332G>T MANE Select ENSP00000325326.2:p.Arg1111Leu
NM_022095.3:c.3332G>T NP_071378.1:p.Arg1111Leu
ENST00000322927.2:c.3332G>T ENSP00000325326.2:p.Arg1111Leu
XM_005260504.3:c.3329G>T XP_005260561.1:p.Arg1110Leu
XM_005260504.4:c.3329G>T XP_005260561.1:p.Arg1110Leu
XM_005260506.2:c.2804G>T XP_005260563.1:p.Arg935Leu
XM_017028012.1:c.2804G>T XP_016883501.1:p.Arg935Leu
XR_002958500.1:n.5279G>T
XR_002958501.1:n.3728G>T
XR_936602.3:n.3843G>T