Canonical Allele Identifier: CA2838361066
Gene: ZNF335 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45954005C>G , CM000682.2:g.45954005C>G GRCh38
NC_000020.10:g.44582644C>G , CM000682.1:g.44582644C>G GRCh37
NC_000020.9:g.44016051C>G NCBI36
NG_029772.1:g.23190G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000322927.3:c.2443-57G>C MANE Select ENSP00000325326.2:n.2443-57G>C
ENST00000322927.2:c.2443-57G>C ENSP00000325326.2:n.2443-57G>C
NM_022095.3:c.2443-57G>C NP_071378.1:n.2443-57G>C
XM_005260504.3:c.2440-57G>C XP_005260561.1:n.2440-57G>C
XM_005260506.2:c.1915-57G>C XP_005260563.1:n.1915-57G>C
XM_011528979.1:c.2443-57G>C XP_011527281.1:n.2443-57G>C
XR_936602.1:n.2954-57G>C
XR_936603.1:n.2860-57G>C
XR_936604.1:n.2977-57G>C
XM_005260504.4:c.2440-57G>C XP_005260561.1:n.2440-57G>C
XM_011528979.3:c.2443-57G>C XP_011527281.1:n.2443-57G>C
XM_017028012.1:c.1915-57G>C XP_016883501.1:n.1915-57G>C
XR_001754372.2:n.2839-57G>C
XR_002958500.1:n.2839-57G>C
XR_002958501.1:n.2839-57G>C
XR_936602.3:n.2934-57G>C
XR_936604.3:n.2956-57G>C
NM_022095.4:c.2443-57G>C MANE Select NP_071378.1:n.2443-57G>C