Canonical Allele Identifier: CA1572628349

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111119088T= , CM000667.2:g.111119088T=	GRCh38
NC_000005.9:g.110454786T= , CM000667.1:g.110454786T=	GRCh37
NC_000005.8:g.110482685T=	NCBI36
NG_008979.1:g.31917T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1872T= MANE Select	ENSP00000424628.3:p.Thr624=
ENST00000506538.6:c.2040T=	ENSP00000423067.2:p.Thr680=
ENST00000513710.3:c.1872T=	ENSP00000424628.3:p.Thr624=
ENST00000612402.4:c.2040T=	ENSP00000479950.1:p.Thr680=
NM_139281.2:c.2040T=	NP_644810.1:p.Thr680=
XM_011543163.1:c.2040T=	XP_011541465.1:p.Thr680=
NM_139281.3:c.1872T= MANE Select	NP_644810.2:p.Thr624=