Canonical Allele Identifier: CA2216306940

Gene: PAGR1 MVP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.29821568T= , CM000678.2:g.29821568T=	GRCh38
NC_000016.9:g.29832889T= , CM000678.1:g.29832889T=	GRCh37
NC_000016.8:g.29740390T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000320330.8:c.*1814T= (PAGR1) MANE Select	ENSP00000326519.6:n.*1814T=
ENST00000357402.10:c.-36+1058T= (MVP) MANE Select	ENSP00000349977.5:n.-36+1058T=
ENST00000357402.9:c.-36+1058T= (MVP)	ENSP00000349977.5:n.-36+1058T=
ENST00000395353.5:c.-77+1058T= (MVP)	ENSP00000378760.1:n.-77+1058T=
ENST00000562285.1:c.402+1666T=
ENST00000562463.5:c.-36+1058T= (MVP)	ENSP00000457734.1:n.-36+1058T=
ENST00000563096.1:n.45+1058T= (MVP)
ENST00000563558.5:c.-77+1058T= (MVP)	ENSP00000454825.1:n.-77+1058T=
ENST00000563915.5:c.-77+1058T= (MVP)	ENSP00000455819.1:n.-77+1058T=
ENST00000565164.1:c.-36+195T= (MVP)	ENSP00000454819.1:n.-36+195T=
ENST00000565830.5:n.34+1058T= (MVP)
ENST00000566066.5:c.-228+1058T= (MVP)	ENSP00000455186.1:n.-228+1058T=
ENST00000566859.5:c.-36+1058T= (MVP)	ENSP00000455741.1:n.-36+1058T=
ENST00000569887.1:c.-36+1058T= (MVP)	ENSP00000455532.1:n.-36+1058T=
ENST00000570234.5:c.-146+177T= (MVP)	ENSP00000456291.1:n.-146+177T=
NM_005115.4:c.-36+1058T= (MVP)	NP_005106.2:n.-36+1058T=
NM_017458.3:c.-77+1058T= (MVP)	NP_059447.2:n.-77+1058T=
NM_024516.3:c.*1814T= (PAGR1)	NP_078792.1:n.*1814T=
NM_005115.5:c.-36+1058T= (MVP) MANE Select	NP_005106.2:n.-36+1058T=
NM_024516.4:c.*1814T= (PAGR1) MANE Select	NP_078792.1:n.*1814T=