Canonical Allele Identifier: CA1947177942

Gene: PHRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.611919C= , CM000673.2:g.611919C=	GRCh38
NC_000011.9:g.611919C= , CM000673.1:g.611919C=	GRCh37
NC_000011.8:g.601919C=	NCBI36
NG_029106.1:g.9081G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001286581.2:c.*142C= MANE Select	NP_001273510.1:n.*142C=
ENST00000264555.10:c.*142C= MANE Select	ENSP00000264555.5:n.*142C=
NM_001286581.1:c.*142C=	NP_001273510.1:n.*142C=
NM_001286582.1:c.*142C=	NP_001273511.1:n.*142C=
NM_001286582.2:c.*142C=	NP_001273511.1:n.*142C=
NM_001286583.1:c.*142C=	NP_001273512.1:n.*142C=
NM_001286583.2:c.*142C=	NP_001273512.1:n.*142C=
NM_020901.3:c.*142C=	NP_065952.2:n.*142C=
NM_020901.4:c.*142C=	NP_065952.2:n.*142C=
ENST00000264555.9:c.*142C=	ENSP00000264555.5:n.*142C=
ENST00000413872.6:c.*142C=	ENSP00000388589.2:n.*142C=
ENST00000416188.2:c.*142C=	ENSP00000410626.2:n.*142C=
ENST00000416188.3:c.*142C=	ENSP00000410626.2:n.*142C=
ENST00000533464.5:c.*142C=	ENSP00000431870.1:n.*142C=
ENST00000534320.5:c.*441C=	ENSP00000435360.1:n.*441C=
XM_005253025.3:c.*142C=	XP_005253082.1:n.*142C=
XM_005253025.5:c.*142C=	XP_005253082.1:n.*142C=
XM_005253027.2:c.*142C=	XP_005253084.1:n.*142C=
XM_005253027.3:c.*142C=	XP_005253084.1:n.*142C=
XM_011520236.1:c.*142C=	XP_011518538.1:n.*142C=
XM_011520236.3:c.*142C=	XP_011518538.1:n.*142C=
XM_011520237.1:c.*142C=	XP_011518539.1:n.*142C=
XM_011520237.3:c.*142C=	XP_011518539.1:n.*142C=