Canonical Allele Identifier: CA976226435

Gene: PAGR1 MVP

Linked Data

• dbSNP Id: rs2067361611
• gnomAD v3: 16-29821568-T-TAC
• gnomAD v4: 16-29821568-T-TAC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.29821572_29821573dup , CM000678.2:g.29821572_29821573dup	GRCh38
NC_000016.9:g.29832893_29832894dup , CM000678.1:g.29832893_29832894dup	GRCh37
NC_000016.8:g.29740394_29740395dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320330.8:c.*1818_*1819dup (PAGR1) MANE Select	ENSP00000326519.6:n.*1818_*1819dup
ENST00000357402.10:c.-36+1062_-36+1063dup (MVP) MANE Select	ENSP00000349977.5:n.-36+1062_-36+1063dup
ENST00000357402.9:c.-36+1062_-36+1063dup (MVP)	ENSP00000349977.5:n.-36+1062_-36+1063dup
ENST00000395353.5:c.-77+1062_-77+1063dup (MVP)	ENSP00000378760.1:n.-77+1062_-77+1063dup
ENST00000562285.1:c.402+1670_402+1671dup
ENST00000562463.5:c.-36+1062_-36+1063dup (MVP)	ENSP00000457734.1:n.-36+1062_-36+1063dup
ENST00000563096.1:n.45+1062_45+1063dup (MVP)
ENST00000563558.5:c.-77+1062_-77+1063dup (MVP)	ENSP00000454825.1:n.-77+1062_-77+1063dup
ENST00000563915.5:c.-77+1062_-77+1063dup (MVP)	ENSP00000455819.1:n.-77+1062_-77+1063dup
ENST00000565164.1:c.-36+199_-36+200dup (MVP)	ENSP00000454819.1:n.-36+199_-36+200dup
ENST00000565830.5:n.34+1062_34+1063dup (MVP)
ENST00000566066.5:c.-228+1062_-228+1063dup (MVP)	ENSP00000455186.1:n.-228+1062_-228+1063dup
ENST00000566859.5:c.-36+1062_-36+1063dup (MVP)	ENSP00000455741.1:n.-36+1062_-36+1063dup
ENST00000569887.1:c.-36+1062_-36+1063dup (MVP)	ENSP00000455532.1:n.-36+1062_-36+1063dup
ENST00000570234.5:c.-146+181_-146+182dup (MVP)	ENSP00000456291.1:n.-146+181_-146+182dup
NM_005115.4:c.-36+1062_-36+1063dup (MVP)	NP_005106.2:n.-36+1062_-36+1063dup
NM_017458.3:c.-77+1062_-77+1063dup (MVP)	NP_059447.2:n.-77+1062_-77+1063dup
NM_024516.3:c.*1818_*1819dup (PAGR1)	NP_078792.1:n.*1818_*1819dup
NM_005115.5:c.-36+1062_-36+1063dup (MVP) MANE Select	NP_005106.2:n.-36+1062_-36+1063dup
NM_024516.4:c.*1818_*1819dup (PAGR1) MANE Select	NP_078792.1:n.*1818_*1819dup