Canonical Allele Identifier: CA280420919

Gene: PAGR1 MVP

Linked Data

• dbSNP Id: rs553472172
• gnomAD v3: 16-29821591-T-C
• gnomAD v4: 16-29821591-T-C
• MyVariant Identifiers: chr16:g.29832912T>C (hg19) ; chr16:g.29821591T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.29821591T>C , CM000678.2:g.29821591T>C	GRCh38
NC_000016.9:g.29832912T>C , CM000678.1:g.29832912T>C	GRCh37
NC_000016.8:g.29740413T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000320330.8:c.*1837T>C (PAGR1) MANE Select	ENSP00000326519.6:n.*1837T>C
ENST00000357402.10:c.-36+1081T>C (MVP) MANE Select	ENSP00000349977.5:n.-36+1081T>C
ENST00000357402.9:c.-36+1081T>C (MVP)	ENSP00000349977.5:n.-36+1081T>C
ENST00000395353.5:c.-77+1081T>C (MVP)	ENSP00000378760.1:n.-77+1081T>C
ENST00000562285.1:c.402+1689T>C
ENST00000562463.5:c.-36+1081T>C (MVP)	ENSP00000457734.1:n.-36+1081T>C
ENST00000563096.1:n.45+1081T>C (MVP)
ENST00000563558.5:c.-77+1081T>C (MVP)	ENSP00000454825.1:n.-77+1081T>C
ENST00000563915.5:c.-77+1081T>C (MVP)	ENSP00000455819.1:n.-77+1081T>C
ENST00000565164.1:c.-36+218T>C (MVP)	ENSP00000454819.1:n.-36+218T>C
ENST00000565830.5:n.34+1081T>C (MVP)
ENST00000566066.5:c.-228+1081T>C (MVP)	ENSP00000455186.1:n.-228+1081T>C
ENST00000566859.5:c.-36+1081T>C (MVP)	ENSP00000455741.1:n.-36+1081T>C
ENST00000569887.1:c.-36+1081T>C (MVP)	ENSP00000455532.1:n.-36+1081T>C
ENST00000570234.5:c.-146+200T>C (MVP)	ENSP00000456291.1:n.-146+200T>C
NM_005115.4:c.-36+1081T>C (MVP)	NP_005106.2:n.-36+1081T>C
NM_017458.3:c.-77+1081T>C (MVP)	NP_059447.2:n.-77+1081T>C
NM_024516.3:c.*1837T>C (PAGR1)	NP_078792.1:n.*1837T>C
NM_005115.5:c.-36+1081T>C (MVP) MANE Select	NP_005106.2:n.-36+1081T>C
NM_024516.4:c.*1837T>C (PAGR1) MANE Select	NP_078792.1:n.*1837T>C