Canonical Allele Identifier: CA1572628284
Gene: WDR36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111118957_111118958delinsAT , CM000667.2:g.111118957_111118958delinsAT GRCh38
NC_000005.9:g.110454655_110454656delinsAT , CM000667.1:g.110454655_110454656delinsAT GRCh37
NC_000005.8:g.110482554_110482555delinsAT NCBI36
NG_008979.1:g.31786_31787delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1797-56_1797-55delinsAT MANE Select ENSP00000424628.3:n.1797-56_1797-55delins...
ENST00000506538.6:c.1965-56_1965-55delinsAT ENSP00000423067.2:n.1965-56_1965-55delins...
ENST00000513710.3:c.1797-56_1797-55delinsAT ENSP00000424628.3:n.1797-56_1797-55delins...
ENST00000612402.4:c.1965-56_1965-55delinsAT ENSP00000479950.1:n.1965-56_1965-55delins...
NM_139281.2:c.1965-56_1965-55delinsAT NP_644810.1:n.1965-56_1965-55delinsAT
XM_011543163.1:c.1965-56_1965-55delinsAT XP_011541465.1:n.1965-56_1965-55delinsAT
NM_139281.3:c.1797-56_1797-55delinsAT MANE Select NP_644810.2:n.1797-56_1797-55delinsAT