Canonical Allele Identifier: CA1321706629

Gene: WDR12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202888349T= , CM000664.2:g.202888349T=	GRCh38
NC_000002.11:g.203753072T= , CM000664.1:g.203753072T=	GRCh37
NC_000002.10:g.203461317T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018256.4:c.742-3814A= MANE Select	NP_060726.3:n.742-3814A=
ENST00000261015.5:c.742-3814A= MANE Select	ENSP00000261015.4:n.742-3814A=
NM_001371664.1:c.328-3814A=	NP_001358593.1:n.328-3814A=
NM_018256.3:c.742-3814A=	NP_060726.3:n.742-3814A=
ENST00000261015.4:c.742-3814A=	ENSP00000261015.3:n.742-3814A=
ENST00000475611.1:n.272-3814A=
ENST00000477727.5:n.59-3814A=
ENST00000688520.1:c.742-3814A=	ENSP00000509107.1:n.742-3814A=
XM_011511469.1:c.328-3814A=	XP_011509771.1:n.328-3814A=
XM_011511469.3:c.328-3814A=	XP_011509771.1:n.328-3814A=