Canonical Allele Identifier: CA1321698338

Gene: WDR12

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202881162T= , CM000664.2:g.202881162T=	GRCh38
NC_000002.11:g.203745885T= , CM000664.1:g.203745885T=	GRCh37
NC_000002.10:g.203454130T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688520.1:c.1195-225A=	ENSP00000509107.1:n.1195-225A=
ENST00000261015.5:c.1195-225A= MANE Select	ENSP00000261015.4:n.1195-225A=
ENST00000261015.4:c.1195-225A=	ENSP00000261015.3:n.1195-225A=
ENST00000467777.1:n.146-225A=
NM_018256.3:c.1195-225A=	NP_060726.3:n.1195-225A=
XM_011511469.1:c.781-225A=	XP_011509771.1:n.781-225A=
XM_011511469.3:c.781-225A=	XP_011509771.1:n.781-225A=
NM_001371664.1:c.781-225A=	NP_001358593.1:n.781-225A=
NM_018256.4:c.1195-225A= MANE Select	NP_060726.3:n.1195-225A=