Canonical Allele Identifier: CA10654442

Gene: PIGV

Linked Data

• ClinVar Variation Id: 368873
• ClinVar RCV Id: RCV000339893
• dbSNP Id: rs71636780
• gnomAD v2: 1-27114447-G-A
• gnomAD v3: 1-26787956-G-A
• gnomAD v4: 1-26787956-G-A
• MyVariant Identifiers: chr1:g.27114447G>A (hg19) ; chr1:g.26787956G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26787956G>A , CM000663.2:g.26787956G>A	GRCh38
NC_000001.10:g.27114447G>A , CM000663.1:g.27114447G>A	GRCh37
NC_000001.9:g.26987034G>A	NCBI36
NG_028133.1:g.4994G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000686194.1:c.-58+150G>A	ENSP00000509240.1:n.-58+150G>A
ENST00000686655.1:c.-70G>A	ENSP00000510382.1:n.-70G>A
ENST00000688522.1:c.-370G>A	ENSP00000508665.1:n.-370G>A
ENST00000688730.1:c.-337G>A	ENSP00000508720.1:n.-337G>A
ENST00000691454.1:c.-91G>A	ENSP00000509275.1:n.-91G>A
ENST00000693629.1:c.-91G>A	ENSP00000509280.1:n.-91G>A
ENST00000455364.2:c.-58+738G>A	ENSP00000406080.2:n.-58+738G>A
ENST00000674202.1:c.-370G>A MANE Select	ENSP00000501479.1:n.-370G>A
ENST00000674335.1:c.-304+150G>A	ENSP00000501446.1:n.-304+150G>A
ENST00000430292.5:c.-58+150G>A	ENSP00000399067.1:n.-58+150G>A
NM_001374478.1:c.-58+738G>A	NP_001361407.1:n.-58+738G>A
NM_001374480.1:c.-91G>A	NP_001361409.1:n.-91G>A
NM_001374481.1:c.-58+150G>A	NP_001361410.1:n.-58+150G>A
NM_001374483.1:c.-304+150G>A	NP_001361412.1:n.-304+150G>A
NM_001374484.1:c.-58+150G>A	NP_001361413.1:n.-58+150G>A
NM_001374486.1:c.-370G>A	NP_001361415.1:n.-370G>A
NM_017837.4:c.-370G>A MANE Select	NP_060307.2:n.-370G>A
NR_164651.1:n.408G>A
NR_164652.1:n.7G>A