Canonical Allele Identifier: CA2178932552

Gene: PRTG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.55657884C= , CM000677.2:g.55657884C=	GRCh38
NC_000015.9:g.55950082C= , CM000677.1:g.55950082C=	GRCh37
NC_000015.8:g.53737374C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_173814.6:c.2041+14561G= MANE Select	NP_776175.2:n.2041+14561G=
ENST00000389286.9:c.2041+14561G= MANE Select	ENSP00000373937.4:n.2041+14561G=
NM_173814.5:c.2041+14561G=	NP_776175.2:n.2041+14561G=
ENST00000389286.8:c.2041+14561G=	ENSP00000373937.4:n.2041+14561G=
ENST00000561465.1:c.647-1530G=	ENSP00000453160.1:n.647-1530G=
XM_011521459.1:c.2042-1508G=	XP_011519761.1:n.2042-1508G=
XM_011521459.2:c.2042-1508G=	XP_011519761.1:n.2042-1508G=
XM_011521460.1:c.2042-1530G=	XP_011519762.1:n.2042-1530G=
XM_011521460.2:c.2042-1530G=	XP_011519762.1:n.2042-1530G=
XM_017022081.2:c.1807+14561G=	XP_016877570.1:n.1807+14561G=
XM_017022082.2:c.2041+14561G=	XP_016877571.1:n.2041+14561G=
XR_429451.1:n.2759+14561G=
XR_931797.1:n.2316+14561G=