Canonical Allele Identifier: CA2674832921

Gene: WDR36

Linked Data

• gnomAD v4: 5-111119169-T-TTAGATTGTTTTGGGATGAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111119169_111119170insTAGATTGTTTTGGGATGAAG , CM000667.2:g.111119169_111119170insTAGATTGTTTTGGGATGAAG	GRCh38
NC_000005.9:g.110454867_110454868insTAGATTGTTTTGGGATGAAG , CM000667.1:g.110454867_110454868insTAGATTGTTTTGGGATGAAG	GRCh37
NC_000005.8:g.110482766_110482767insTAGATTGTTTTGGGATGAAG	NCBI36
NG_008979.1:g.31998_31999insTAGATTGTTTTGGGATGAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1904+49_1904+50insTAGATTGTTTTGGGATGAAG MANE Select	ENSP00000424628.3:n.1904+49_1904+50insTAGATTGTTTTGGGATGAAG
ENST00000506538.6:c.2072+49_2072+50insTAGATTGTTTTGGGATGAAG	ENSP00000423067.2:n.2072+49_2072+50insTAGATTGTTTTGGGATGAAG
ENST00000513710.3:c.1904+49_1904+50insTAGATTGTTTTGGGATGAAG	ENSP00000424628.3:n.1904+49_1904+50insTAGATTGTTTTGGGATGAAG
ENST00000612402.4:c.2072+49_2072+50insTAGATTGTTTTGGGATGAAG	ENSP00000479950.1:n.2072+49_2072+50insTAGATTGTTTTGGGATGAAG
NM_139281.2:c.2072+49_2072+50insTAGATTGTTTTGGGATGAAG	NP_644810.1:n.2072+49_2072+50insTAGATTGTTTTGGGATGAAG
XM_011543163.1:c.2072+49_2072+50insTAGATTGTTTTGGGATGAAG	XP_011541465.1:n.2072+49_2072+50insTAGATTGTTTTGGGATGAAG
NM_139281.3:c.1904+49_1904+50insTAGATTGTTTTGGGATGAAG MANE Select	NP_644810.2:n.1904+49_1904+50insTAGATTGTTTTGGGATGAAG