Canonical Allele Identifier: CA2674832842

Gene: WDR36

Linked Data

• gnomAD v4: 5-111118923-A-ATCCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111118925_111118929dup , CM000667.2:g.111118925_111118929dup	GRCh38
NC_000005.9:g.110454623_110454627dup , CM000667.1:g.110454623_110454627dup	GRCh37
NC_000005.8:g.110482522_110482526dup	NCBI36
NG_008979.1:g.31754_31758dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1797-88_1797-84dup MANE Select	ENSP00000424628.3:n.1797-88_1797-84dup
ENST00000506538.6:c.1965-88_1965-84dup	ENSP00000423067.2:n.1965-88_1965-84dup
ENST00000513710.3:c.1797-88_1797-84dup	ENSP00000424628.3:n.1797-88_1797-84dup
ENST00000612402.4:c.1965-88_1965-84dup	ENSP00000479950.1:n.1965-88_1965-84dup
NM_139281.2:c.1965-88_1965-84dup	NP_644810.1:n.1965-88_1965-84dup
XM_011543163.1:c.1965-88_1965-84dup	XP_011541465.1:n.1965-88_1965-84dup
NM_139281.3:c.1797-88_1797-84dup MANE Select	NP_644810.2:n.1797-88_1797-84dup