Canonical Allele Identifier: CA1160223185
Gene: PIGV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26790813A= , CM000663.2:g.26790813A= GRCh38
NC_000001.10:g.27117304A= , CM000663.1:g.27117304A= GRCh37
NC_000001.9:g.26989891A= NCBI36
NG_028133.1:g.7851A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000686194.1:c.-3A= ENSP00000509240.1:n.-3A=
ENST00000686325.1:c.-3A= ENSP00000509836.1:n.-3A=
ENST00000686422.1:n.908A=
ENST00000686655.1:c.-37+2824A= ENSP00000510382.1:n.-37+2824A=
ENST00000687468.1:c.-3A= ENSP00000510051.1:n.-3A=
ENST00000688522.1:c.-3A= ENSP00000508665.1:n.-3A=
ENST00000688730.1:c.-304+2824A= ENSP00000508720.1:n.-304+2824A=
ENST00000689130.1:c.-304+2824A= ENSP00000509671.1:n.-304+2824A=
ENST00000691135.1:c.-3A= ENSP00000510357.1:n.-3A=
ENST00000691454.1:c.-3A= ENSP00000509275.1:n.-3A=
ENST00000693629.1:c.-3A= ENSP00000509280.1:n.-3A=
ENST00000078527.9:c.-3A= ENSP00000078527.4:n.-3A=
ENST00000374145.6:c.-3A= ENSP00000363260.1:n.-3A=
ENST00000431541.6:c.-3A= ENSP00000388425.2:n.-3A=
ENST00000455364.2:c.-3A= ENSP00000406080.2:n.-3A=
ENST00000674202.1:c.-3A= MANE Select ENSP00000501479.1:n.-3A=
ENST00000674222.1:c.-3A= ENSP00000501335.1:n.-3A=
ENST00000674273.1:c.-3A= ENSP00000501527.1:n.-3A=
ENST00000674317.1:n.303A=
ENST00000674335.1:c.-304+3007A= ENSP00000501446.1:n.-304+3007A=
ENST00000078527.8:c.-3A= ENSP00000078527.4:n.-3A=
ENST00000374145.5:c.-3A= ENSP00000363260.1:n.-3A=
ENST00000430292.5:c.-3A= ENSP00000399067.1:n.-3A=
ENST00000431541.5:c.-3A= ENSP00000388425.1:n.-3A=
ENST00000455364.1:c.-3A= ENSP00000406080.1:n.-3A=
ENST00000472757.5:c.-3A= ENSP00000436884.1:n.-3A=
NM_001202554.1:c.-3A= NP_001189483.1:n.-3A=
NM_017837.3:c.-3A= NP_060307.2:n.-3A=
NM_001202554.2:c.-3A= NP_001189483.1:n.-3A=
NM_001374478.1:c.-3A= NP_001361407.1:n.-3A=
NM_001374480.1:c.-3A= NP_001361409.1:n.-3A=
NM_001374481.1:c.-3A= NP_001361410.1:n.-3A=
NM_001374482.1:c.-3A= NP_001361411.1:n.-3A=
NM_001374483.1:c.-304+3007A= NP_001361412.1:n.-304+3007A=
NM_001374484.1:c.-3A= NP_001361413.1:n.-3A=
NM_001374485.1:c.-3A= NP_001361414.1:n.-3A=
NM_001374486.1:c.-3A= NP_001361415.1:n.-3A=
NM_017837.4:c.-3A= MANE Select NP_060307.2:n.-3A=
NR_164651.1:n.496A=
NR_164652.1:n.374A=