Canonical Allele Identifier: CA2674832829

Gene: WDR36

Linked Data

• gnomAD v4: 5-111118892-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111118899_111118900del , CM000667.2:g.111118899_111118900del	GRCh38
NC_000005.9:g.110454597_110454598del , CM000667.1:g.110454597_110454598del	GRCh37
NC_000005.8:g.110482496_110482497del	NCBI36
NG_008979.1:g.31728_31729del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1797-114_1797-113del MANE Select	ENSP00000424628.3:n.1797-114_1797-113del
ENST00000506538.6:c.1965-114_1965-113del	ENSP00000423067.2:n.1965-114_1965-113del
ENST00000513710.3:c.1797-114_1797-113del	ENSP00000424628.3:n.1797-114_1797-113del
ENST00000612402.4:c.1965-114_1965-113del	ENSP00000479950.1:n.1965-114_1965-113del
NM_139281.2:c.1965-114_1965-113del	NP_644810.1:n.1965-114_1965-113del
XM_011543163.1:c.1965-114_1965-113del	XP_011541465.1:n.1965-114_1965-113del
NM_139281.3:c.1797-114_1797-113del MANE Select	NP_644810.2:n.1797-114_1797-113del