Canonical Allele Identifier: CA1986951760

Gene: PCF11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.83165228T= , CM000673.2:g.83165228T=	GRCh38
NC_000011.9:g.82876270T= , CM000673.1:g.82876270T=	GRCh37
NC_000011.8:g.82553918T=	NCBI36
NG_051805.1:g.13134T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001346413.3:c.703-372T= MANE Select	NP_001333342.1:n.703-372T=
ENST00000690938.1:c.703-372T= MANE Select	ENSP00000508500.1:n.703-372T=
NM_001346413.1:c.703-372T=	NP_001333342.1:n.703-372T=
NM_001346413.2:c.703-372T=	NP_001333342.1:n.703-372T=
NM_001346414.1:c.703-372T=	NP_001333343.1:n.703-372T=
NM_001346414.2:c.703-372T=	NP_001333343.1:n.703-372T=
NM_001346415.1:c.703-372T=	NP_001333344.1:n.703-372T=
NM_001346415.2:c.703-372T=	NP_001333344.1:n.703-372T=
NM_015885.3:c.703-372T=	NP_056969.2:n.703-372T=
NM_015885.4:c.703-372T=	NP_056969.2:n.703-372T=
ENST00000298281.8:c.703-372T=	ENSP00000298281.4:n.703-372T=
ENST00000530304.5:c.703-372T=	ENSP00000431567.1:n.703-372T=
ENST00000530660.5:c.703-372T=	ENSP00000434540.1:n.703-372T=
ENST00000620955.1:c.703-372T=	ENSP00000479505.1:n.703-372T=
XM_005274048.1:c.703-372T=	XP_005274105.1:n.703-372T=
XM_005274049.1:c.703-372T=	XP_005274106.1:n.703-372T=
XR_001747905.1:n.1048-372T=
XR_001747906.1:n.1048-372T=