Canonical Allele Identifier: CA801886275
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs1289596144
gnomAD v3: 5-111118892-T-TA
gnomAD v4: 5-111118892-T-TA
MyVariant Identifiers: chr5:g.110454590_110454591insA (hg19) chr5:g.111118892_111118893insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111118900dup , CM000667.2:g.111118900dup GRCh38
NC_000005.9:g.110454598dup , CM000667.1:g.110454598dup GRCh37
NC_000005.8:g.110482497dup NCBI36
NG_008979.1:g.31729dup

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1797-113dup MANE Select ENSP00000424628.3:n.1797-113dup
ENST00000506538.6:c.1965-113dup ENSP00000423067.2:n.1965-113dup
ENST00000513710.3:c.1797-113dup ENSP00000424628.3:n.1797-113dup
ENST00000612402.4:c.1965-113dup ENSP00000479950.1:n.1965-113dup
NM_139281.2:c.1965-113dup NP_644810.1:n.1965-113dup
XM_011543163.1:c.1965-113dup XP_011541465.1:n.1965-113dup
NM_139281.3:c.1797-113dup MANE Select NP_644810.2:n.1797-113dup
Search 100 bp 5'
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