Canonical Allele Identifier: CA1572628308
Gene: WDR36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111118996_111119000delinsGTTAA , CM000667.2:g.111118996_111119000delinsGTTAA GRCh38
NC_000005.9:g.110454694_110454698delinsGTTAA , CM000667.1:g.110454694_110454698delinsGTTAA GRCh37
NC_000005.8:g.110482593_110482597delinsGTTAA NCBI36
NG_008979.1:g.31825_31829delinsGTTAA

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1797-17_1797-13delinsGTTAA MANE Select ENSP00000424628.3:n.1797-17_1797-13delins...
ENST00000506538.6:c.1965-17_1965-13delinsGTTAA ENSP00000423067.2:n.1965-17_1965-13delins...
ENST00000513710.3:c.1797-17_1797-13delinsGTTAA ENSP00000424628.3:n.1797-17_1797-13delins...
ENST00000612402.4:c.1965-17_1965-13delinsGTTAA ENSP00000479950.1:n.1965-17_1965-13delins...
NM_139281.2:c.1965-17_1965-13delinsGTTAA NP_644810.1:n.1965-17_1965-13delinsGTTAA
XM_011543163.1:c.1965-17_1965-13delinsGTTAA XP_011541465.1:n.1965-17_1965-13delinsGTT...
NM_139281.3:c.1797-17_1797-13delinsGTTAA MANE Select NP_644810.2:n.1797-17_1797-13delinsGTTAA