Canonical Allele Identifier: CA2674832857
Gene: WDR36 HGNC NCBI

Linked Data

gnomAD v4: 5-111118952-TGTGAA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111118953_111118957del , CM000667.2:g.111118953_111118957del GRCh38
NC_000005.9:g.110454651_110454655del , CM000667.1:g.110454651_110454655del GRCh37
NC_000005.8:g.110482550_110482554del NCBI36
NG_008979.1:g.31782_31786del

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1797-60_1797-56del MANE Select ENSP00000424628.3:n.1797-60_1797-56del
ENST00000506538.6:c.1965-60_1965-56del ENSP00000423067.2:n.1965-60_1965-56del
ENST00000513710.3:c.1797-60_1797-56del ENSP00000424628.3:n.1797-60_1797-56del
ENST00000612402.4:c.1965-60_1965-56del ENSP00000479950.1:n.1965-60_1965-56del
NM_139281.2:c.1965-60_1965-56del NP_644810.1:n.1965-60_1965-56del
XM_011543163.1:c.1965-60_1965-56del XP_011541465.1:n.1965-60_1965-56del
NM_139281.3:c.1797-60_1797-56del MANE Select NP_644810.2:n.1797-60_1797-56del
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