Canonical Allele Identifier: CA1160223245

Gene: PIGV

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26790993_26790994delinsCT , CM000663.2:g.26790993_26790994delinsCT	GRCh38
NC_000001.10:g.27117484_27117485delinsCT , CM000663.1:g.27117484_27117485delinsCT	GRCh37
NC_000001.9:g.26990071_26990072delinsCT	NCBI36
NG_028133.1:g.8031_8032delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686194.1:c.78+100_78+101delinsCT	ENSP00000509240.1:n.78+100_78+101delinsCT
ENST00000686325.1:c.78+100_78+101delinsCT	ENSP00000509836.1:n.78+100_78+101delinsCT
ENST00000686422.1:n.988+100_988+101delinsCT
ENST00000686655.1:c.-37+3004_-37+3005delinsCT	ENSP00000510382.1:n.-37+3004_-37+3005delinsCT
ENST00000687468.1:c.78+100_78+101delinsCT	ENSP00000510051.1:n.78+100_78+101delinsCT
ENST00000688522.1:c.78+100_78+101delinsCT	ENSP00000508665.1:n.78+100_78+101delinsCT
ENST00000688730.1:c.-304+3004_-304+3005delinsCT	ENSP00000508720.1:n.-304+3004_-304+3005delinsCT
ENST00000689130.1:c.-304+3004_-304+3005delinsCT	ENSP00000509671.1:n.-304+3004_-304+3005delinsCT
ENST00000691135.1:c.78+100_78+101delinsCT	ENSP00000510357.1:n.78+100_78+101delinsCT
ENST00000691454.1:c.78+100_78+101delinsCT	ENSP00000509275.1:n.78+100_78+101delinsCT
ENST00000693629.1:c.78+100_78+101delinsCT	ENSP00000509280.1:n.78+100_78+101delinsCT
ENST00000078527.9:c.78+100_78+101delinsCT	ENSP00000078527.4:n.78+100_78+101delinsCT
ENST00000374145.6:c.78+100_78+101delinsCT	ENSP00000363260.1:n.78+100_78+101delinsCT
ENST00000431541.6:c.78+100_78+101delinsCT	ENSP00000388425.2:n.78+100_78+101delinsCT
ENST00000455364.2:c.78+100_78+101delinsCT	ENSP00000406080.2:n.78+100_78+101delinsCT
ENST00000674202.1:c.78+100_78+101delinsCT MANE Select	ENSP00000501479.1:n.78+100_78+101delinsCT
ENST00000674222.1:c.78+100_78+101delinsCT	ENSP00000501335.1:n.78+100_78+101delinsCT
ENST00000674273.1:c.78+100_78+101delinsCT	ENSP00000501527.1:n.78+100_78+101delinsCT
ENST00000674317.1:n.383+100_383+101delinsCT
ENST00000674335.1:c.-303-3120_-303-3119delinsCT	ENSP00000501446.1:n.-303-3120_-303-3119delinsCT
ENST00000078527.8:c.78+100_78+101delinsCT	ENSP00000078527.4:n.78+100_78+101delinsCT
ENST00000374145.5:c.78+100_78+101delinsCT	ENSP00000363260.1:n.78+100_78+101delinsCT
ENST00000430292.5:c.78+100_78+101delinsCT	ENSP00000399067.1:n.78+100_78+101delinsCT
ENST00000431541.5:c.78+100_78+101delinsCT	ENSP00000388425.1:n.78+100_78+101delinsCT
ENST00000455364.1:c.78+100_78+101delinsCT	ENSP00000406080.1:n.78+100_78+101delinsCT
ENST00000472757.5:c.78+100_78+101delinsCT	ENSP00000436884.1:n.78+100_78+101delinsCT
NM_001202554.1:c.78+100_78+101delinsCT	NP_001189483.1:n.78+100_78+101delinsCT
NM_017837.3:c.78+100_78+101delinsCT	NP_060307.2:n.78+100_78+101delinsCT
NM_001202554.2:c.78+100_78+101delinsCT	NP_001189483.1:n.78+100_78+101delinsCT
NM_001374478.1:c.78+100_78+101delinsCT	NP_001361407.1:n.78+100_78+101delinsCT
NM_001374480.1:c.78+100_78+101delinsCT	NP_001361409.1:n.78+100_78+101delinsCT
NM_001374481.1:c.78+100_78+101delinsCT	NP_001361410.1:n.78+100_78+101delinsCT
NM_001374482.1:c.78+100_78+101delinsCT	NP_001361411.1:n.78+100_78+101delinsCT
NM_001374483.1:c.-303-3120_-303-3119delinsCT	NP_001361412.1:n.-303-3120_-303-3119delinsCT
NM_001374484.1:c.78+100_78+101delinsCT	NP_001361413.1:n.78+100_78+101delinsCT
NM_001374485.1:c.78+100_78+101delinsCT	NP_001361414.1:n.78+100_78+101delinsCT
NM_001374486.1:c.78+100_78+101delinsCT	NP_001361415.1:n.78+100_78+101delinsCT
NM_017837.4:c.78+100_78+101delinsCT MANE Select	NP_060307.2:n.78+100_78+101delinsCT
NR_164651.1:n.576+100_576+101delinsCT
NR_164652.1:n.454+100_454+101delinsCT