Canonical Allele Identifier: CA1572628345

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111119079T= , CM000667.2:g.111119079T=	GRCh38
NC_000005.9:g.110454777T= , CM000667.1:g.110454777T=	GRCh37
NC_000005.8:g.110482676T=	NCBI36
NG_008979.1:g.31908T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1863T= MANE Select	ENSP00000424628.3:p.Phe621=
ENST00000506538.6:c.2031T=	ENSP00000423067.2:p.Phe677=
ENST00000513710.3:c.1863T=	ENSP00000424628.3:p.Phe621=
ENST00000612402.4:c.2031T=	ENSP00000479950.1:p.Phe677=
NM_139281.2:c.2031T=	NP_644810.1:p.Phe677=
XM_011543163.1:c.2031T=	XP_011541465.1:p.Phe677=
NM_139281.3:c.1863T= MANE Select	NP_644810.2:p.Phe621=