Canonical Allele Identifier: CA1080096024

Gene: WDR36

Linked Data

• dbSNP Id: rs1753520511
• gnomAD v3: 5-111119349-TA-T
• gnomAD v4: 5-111119349-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111119350del , CM000667.2:g.111119350del	GRCh38
NC_000005.9:g.110455048del , CM000667.1:g.110455048del	GRCh37
NC_000005.8:g.110482947del	NCBI36
NG_008979.1:g.32179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1904+230del MANE Select	ENSP00000424628.3:n.1904+230del
ENST00000506538.6:c.2072+230del	ENSP00000423067.2:n.2072+230del
ENST00000513710.3:c.1904+230del	ENSP00000424628.3:n.1904+230del
ENST00000612402.4:c.2072+230del	ENSP00000479950.1:n.2072+230del
NM_139281.2:c.2072+230del	NP_644810.1:n.2072+230del
XM_011543163.1:c.2072+230del	XP_011541465.1:n.2072+230del
NM_139281.3:c.1904+230del MANE Select	NP_644810.2:n.1904+230del