Canonical Allele Identifier: CA1572628299

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111118983A= , CM000667.2:g.111118983A=	GRCh38
NC_000005.9:g.110454681A= , CM000667.1:g.110454681A=	GRCh37
NC_000005.8:g.110482580A=	NCBI36
NG_008979.1:g.31812A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000513710.4:c.1797-30A= MANE Select	ENSP00000424628.3:n.1797-30A=
ENST00000506538.6:c.1965-30A=	ENSP00000423067.2:n.1965-30A=
ENST00000513710.3:c.1797-30A=	ENSP00000424628.3:n.1797-30A=
ENST00000612402.4:c.1965-30A=	ENSP00000479950.1:n.1965-30A=
NM_139281.2:c.1965-30A=	NP_644810.1:n.1965-30A=
XM_011543163.1:c.1965-30A=	XP_011541465.1:n.1965-30A=
NM_139281.3:c.1797-30A= MANE Select	NP_644810.2:n.1797-30A=