Canonical Allele Identifier: CA2644303122

Gene: PIGV

Linked Data

• gnomAD v4: 1-26790730-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26790730G>C , CM000663.2:g.26790730G>C	GRCh38
NC_000001.10:g.27117221G>C , CM000663.1:g.27117221G>C	GRCh37
NC_000001.9:g.26989808G>C	NCBI36
NG_028133.1:g.7768G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000686194.1:c.-57-29G>C	ENSP00000509240.1:n.-57-29G>C
ENST00000686325.1:c.-57-29G>C	ENSP00000509836.1:n.-57-29G>C
ENST00000686422.1:n.854-29G>C
ENST00000686655.1:c.-37+2741G>C	ENSP00000510382.1:n.-37+2741G>C
ENST00000687468.1:c.-57-29G>C	ENSP00000510051.1:n.-57-29G>C
ENST00000688522.1:c.-57-29G>C	ENSP00000508665.1:n.-57-29G>C
ENST00000688730.1:c.-304+2741G>C	ENSP00000508720.1:n.-304+2741G>C
ENST00000689130.1:c.-304+2741G>C	ENSP00000509671.1:n.-304+2741G>C
ENST00000691135.1:c.-86G>C	ENSP00000510357.1:n.-86G>C
ENST00000691454.1:c.-57-29G>C	ENSP00000509275.1:n.-57-29G>C
ENST00000693629.1:c.-57-29G>C	ENSP00000509280.1:n.-57-29G>C
ENST00000078527.9:c.-57-29G>C	ENSP00000078527.4:n.-57-29G>C
ENST00000374145.6:c.-57-29G>C	ENSP00000363260.1:n.-57-29G>C
ENST00000431541.6:c.-57-29G>C	ENSP00000388425.2:n.-57-29G>C
ENST00000455364.2:c.-57-29G>C	ENSP00000406080.2:n.-57-29G>C
ENST00000674202.1:c.-57-29G>C MANE Select	ENSP00000501479.1:n.-57-29G>C
ENST00000674222.1:c.-57-29G>C	ENSP00000501335.1:n.-57-29G>C
ENST00000674273.1:c.-57-29G>C	ENSP00000501527.1:n.-57-29G>C
ENST00000674317.1:n.249-29G>C
ENST00000674335.1:c.-304+2924G>C	ENSP00000501446.1:n.-304+2924G>C
ENST00000078527.8:c.-57-29G>C	ENSP00000078527.4:n.-57-29G>C
ENST00000374145.5:c.-57-29G>C	ENSP00000363260.1:n.-57-29G>C
ENST00000430292.5:c.-57-29G>C	ENSP00000399067.1:n.-57-29G>C
ENST00000431541.5:c.-57-29G>C	ENSP00000388425.1:n.-57-29G>C
ENST00000455364.1:c.-57-29G>C	ENSP00000406080.1:n.-57-29G>C
ENST00000472757.5:c.-57-29G>C	ENSP00000436884.1:n.-57-29G>C
NM_001202554.1:c.-57-29G>C	NP_001189483.1:n.-57-29G>C
NM_017837.3:c.-57-29G>C	NP_060307.2:n.-57-29G>C
NM_001202554.2:c.-57-29G>C	NP_001189483.1:n.-57-29G>C
NM_001374478.1:c.-57-29G>C	NP_001361407.1:n.-57-29G>C
NM_001374480.1:c.-57-29G>C	NP_001361409.1:n.-57-29G>C
NM_001374481.1:c.-57-29G>C	NP_001361410.1:n.-57-29G>C
NM_001374482.1:c.-57-29G>C	NP_001361411.1:n.-57-29G>C
NM_001374483.1:c.-304+2924G>C	NP_001361412.1:n.-304+2924G>C
NM_001374484.1:c.-57-29G>C	NP_001361413.1:n.-57-29G>C
NM_001374485.1:c.-57-29G>C	NP_001361414.1:n.-57-29G>C
NM_001374486.1:c.-57-29G>C	NP_001361415.1:n.-57-29G>C
NM_017837.4:c.-57-29G>C MANE Select	NP_060307.2:n.-57-29G>C
NR_164651.1:n.442-29G>C
NR_164652.1:n.320-29G>C