Canonical Allele Identifier: CA2177893907

Gene: WDR72

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.53613599A= , CM000677.2:g.53613599A=	GRCh38
NC_000015.9:g.53905796A= , CM000677.1:g.53905796A=	GRCh37
NC_000015.8:g.51693088A=	NCBI36
NG_017034.2:g.151064T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360509.10:c.2872+67T= MANE Select	ENSP00000353699.5:n.2872+67T=
ENST00000360509.9:c.2872+67T=	ENSP00000353699.5:n.2872+67T=
ENST00000396328.5:c.2872+67T=	ENSP00000379619.1:n.2872+67T=
ENST00000557913.5:c.2863+67T=	ENSP00000453378.1:n.2863+67T=
ENST00000559418.5:c.2902+67T=	ENSP00000452765.1:n.2902+67T=
NM_182758.3:c.2872+67T=	NP_877435.3:n.2872+67T=
NR_102334.1:n.3112+67T=
XM_011521433.1:c.2872+67T=	XP_011519735.1:n.2872+67T=
XM_011521434.1:c.2872+67T=	XP_011519736.1:n.2872+67T=
XM_011521435.1:c.2872+67T=	XP_011519737.1:n.2872+67T=
XM_011521436.1:c.2854+67T=	XP_011519738.1:n.2854+67T=
XM_011521437.1:c.2752+67T=	XP_011519739.1:n.2752+67T=
XM_011521433.2:c.2872+67T=	XP_011519735.1:n.2872+67T=
XM_011521435.2:c.2872+67T=	XP_011519737.1:n.2872+67T=
XM_011521436.2:c.2854+67T=	XP_011519738.1:n.2854+67T=
XM_011521437.2:c.2752+67T=	XP_011519739.1:n.2752+67T=
XM_017022061.1:c.2872+67T=	XP_016877550.1:n.2872+67T=
NM_182758.4:c.2872+67T= MANE Select	NP_877435.3:n.2872+67T=
NR_102334.2:n.3112+67T=