Canonical Allele Identifier: CA360613495
Gene: WDR36 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119042C>A , CM000667.2:g.111119042C>A GRCh38
NC_000005.9:g.110454740C>A , CM000667.1:g.110454740C>A GRCh37
NC_000005.8:g.110482639C>A NCBI36
NG_008979.1:g.31871C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1826C>A MANE Select ENSP00000424628.3:p.Ala609Asp
ENST00000506538.6:c.1994C>A ENSP00000423067.2:p.Ala665Asp
ENST00000513710.3:c.1826C>A ENSP00000424628.3:p.Ala609Asp
ENST00000612402.4:c.1994C>A ENSP00000479950.1:p.Ala665Asp
NM_139281.2:c.1994C>A NP_644810.1:p.Ala665Asp
XM_011543163.1:c.1994C>A XP_011541465.1:p.Ala665Asp
NM_139281.3:c.1826C>A MANE Select NP_644810.2:p.Ala609Asp