Canonical Allele Identifier: CA1572628203
Gene: WDR36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111118782_111118786delinsTAGTC , CM000667.2:g.111118782_111118786delinsTAGTC GRCh38
NC_000005.9:g.110454480_110454484delinsTAGTC , CM000667.1:g.110454480_110454484delinsTAGTC GRCh37
NC_000005.8:g.110482379_110482383delinsTAGTC NCBI36
NG_008979.1:g.31611_31615delinsTAGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1797-231_1797-227delinsTAGTC MANE Select ENSP00000424628.3:n.1797-231_1797-227delinsTAGTC
ENST00000506538.6:c.1965-231_1965-227delinsTAGTC ENSP00000423067.2:n.1965-231_1965-227delinsTAGTC
ENST00000513710.3:c.1797-231_1797-227delinsTAGTC ENSP00000424628.3:n.1797-231_1797-227delinsTAGTC
ENST00000612402.4:c.1965-231_1965-227delinsTAGTC ENSP00000479950.1:n.1965-231_1965-227delinsTAGTC
NM_139281.2:c.1965-231_1965-227delinsTAGTC NP_644810.1:n.1965-231_1965-227delinsTAGTC
XM_011543163.1:c.1965-231_1965-227delinsTAGTC XP_011541465.1:n.1965-231_1965-227delinsTAGTC
NM_139281.3:c.1797-231_1797-227delinsTAGTC MANE Select NP_644810.2:n.1797-231_1797-227delinsTAGTC