Canonical Allele Identifier: CA1080095917
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs1753511609

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119000_111119003del , CM000667.2:g.111119000_111119003del GRCh38
NC_000005.9:g.110454698_110454701del , CM000667.1:g.110454698_110454701del GRCh37
NC_000005.8:g.110482597_110482600del NCBI36
NG_008979.1:g.31829_31832del

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1797-13_1797-10del MANE Select ENSP00000424628.3:n.1797-13_1797-10del
ENST00000506538.6:c.1965-13_1965-10del ENSP00000423067.2:n.1965-13_1965-10del
ENST00000513710.3:c.1797-13_1797-10del ENSP00000424628.3:n.1797-13_1797-10del
ENST00000612402.4:c.1965-13_1965-10del ENSP00000479950.1:n.1965-13_1965-10del
NM_139281.2:c.1965-13_1965-10del NP_644810.1:n.1965-13_1965-10del
XM_011543163.1:c.1965-13_1965-10del XP_011541465.1:n.1965-13_1965-10del
NM_139281.3:c.1797-13_1797-10del MANE Select NP_644810.2:n.1797-13_1797-10del