Canonical Allele Identifier: CA1572628302
Gene: WDR36 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111118986_111118987delinsCT , CM000667.2:g.111118986_111118987delinsCT GRCh38
NC_000005.9:g.110454684_110454685delinsCT , CM000667.1:g.110454684_110454685delinsCT GRCh37
NC_000005.8:g.110482583_110482584delinsCT NCBI36
NG_008979.1:g.31815_31816delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1797-27_1797-26delinsCT MANE Select ENSP00000424628.3:n.1797-27_1797-26delins...
ENST00000506538.6:c.1965-27_1965-26delinsCT ENSP00000423067.2:n.1965-27_1965-26delins...
ENST00000513710.3:c.1797-27_1797-26delinsCT ENSP00000424628.3:n.1797-27_1797-26delins...
ENST00000612402.4:c.1965-27_1965-26delinsCT ENSP00000479950.1:n.1965-27_1965-26delins...
NM_139281.2:c.1965-27_1965-26delinsCT NP_644810.1:n.1965-27_1965-26delinsCT
XM_011543163.1:c.1965-27_1965-26delinsCT XP_011541465.1:n.1965-27_1965-26delinsCT
NM_139281.3:c.1797-27_1797-26delinsCT MANE Select NP_644810.2:n.1797-27_1797-26delinsCT
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