Canonical Allele Identifier: CA1572628282
Gene: WDR36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111118955_111118956delinsGA , CM000667.2:g.111118955_111118956delinsGA GRCh38
NC_000005.9:g.110454653_110454654delinsGA , CM000667.1:g.110454653_110454654delinsGA GRCh37
NC_000005.8:g.110482552_110482553delinsGA NCBI36
NG_008979.1:g.31784_31785delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1797-58_1797-57delinsGA MANE Select ENSP00000424628.3:n.1797-58_1797-57delinsGA
ENST00000506538.6:c.1965-58_1965-57delinsGA ENSP00000423067.2:n.1965-58_1965-57delinsGA
ENST00000513710.3:c.1797-58_1797-57delinsGA ENSP00000424628.3:n.1797-58_1797-57delinsGA
ENST00000612402.4:c.1965-58_1965-57delinsGA ENSP00000479950.1:n.1965-58_1965-57delinsGA
NM_139281.2:c.1965-58_1965-57delinsGA NP_644810.1:n.1965-58_1965-57delinsGA
XM_011543163.1:c.1965-58_1965-57delinsGA XP_011541465.1:n.1965-58_1965-57delinsGA
NM_139281.3:c.1797-58_1797-57delinsGA MANE Select NP_644810.2:n.1797-58_1797-57delinsGA