Canonical Allele Identifier: CA124932318

Gene: WDR36

Linked Data

• dbSNP Id: rs745309324
• gnomAD v4: 5-111118944-AAT-A
• MyVariant Identifiers: chr5:g.110454643_110454644del (hg19) ; chr5:g.111118945_111118946del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111118947_111118948del , CM000667.2:g.111118947_111118948del	GRCh38
NC_000005.9:g.110454645_110454646del , CM000667.1:g.110454645_110454646del	GRCh37
NC_000005.8:g.110482544_110482545del	NCBI36
NG_008979.1:g.31776_31777del

Transcript Alleles

HGVS	Amino-acid change
ENST00000513710.4:c.1797-66_1797-65del MANE Select	ENSP00000424628.3:n.1797-66_1797-65del
ENST00000506538.6:c.1965-66_1965-65del	ENSP00000423067.2:n.1965-66_1965-65del
ENST00000513710.3:c.1797-66_1797-65del	ENSP00000424628.3:n.1797-66_1797-65del
ENST00000612402.4:c.1965-66_1965-65del	ENSP00000479950.1:n.1965-66_1965-65del
NM_139281.2:c.1965-66_1965-65del	NP_644810.1:n.1965-66_1965-65del
XM_011543163.1:c.1965-66_1965-65del	XP_011541465.1:n.1965-66_1965-65del
NM_139281.3:c.1797-66_1797-65del MANE Select	NP_644810.2:n.1797-66_1797-65del