Canonical Allele Identifier: CA7288027

Gene: VIPAS39

Linked Data

• ClinVar Variation Id: 498137
• ClinVar RCV Id: RCV000592638
• dbSNP Id: rs141155709
• ExAC: 14:77909501 G / C
• gnomAD v2: 14-77909501-G-C
• gnomAD v3: 14-77443158-G-C
• gnomAD v4: 14-77443158-G-C
• MyVariant Identifiers: chr14:g.77909501G>C (hg19) ; chr14:g.77443158G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77443158G>C , CM000676.2:g.77443158G>C	GRCh38
NC_000014.8:g.77909501G>C , CM000676.1:g.77909501G>C	GRCh37
NC_000014.7:g.76979254G>C	NCBI36
NG_023421.1:g.19483C>G
NG_023421.2:g.19483C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557658.6:c.598-6C>G MANE Select	ENSP00000452191.1:n.598-6C>G
ENST00000327028.8:c.451-6C>G	ENSP00000313098.5:n.451-6C>G
ENST00000343765.6:c.598-6C>G	ENSP00000339122.2:n.598-6C>G
ENST00000448935.6:c.451-6C>G	ENSP00000404815.2:n.451-6C>G
ENST00000553576.5:n.4C>G
ENST00000553691.5:n.488-6C>G
ENST00000553888.5:c.598-6C>G	ENSP00000452181.1:n.598-6C>G
ENST00000555854.1:n.43-6C>G
ENST00000556412.4:c.676-6C>G	ENSP00000451857.1:n.676-6C>G
ENST00000557658.5:c.598-6C>G	ENSP00000452191.1:n.598-6C>G
NM_001193314.1:c.598-6C>G	NP_001180243.1:n.598-6C>G
NM_001193315.1:c.598-6C>G	NP_001180244.1:n.598-6C>G
NM_001193316.1:c.451-6C>G	NP_001180245.1:n.451-6C>G
NM_001193317.1:c.598-6C>G	NP_001180246.1:n.598-6C>G
NM_022067.3:c.598-6C>G	NP_071350.2:n.598-6C>G
XM_011537066.1:c.505-6C>G	XP_011535368.1:n.505-6C>G
XM_011537066.2:c.505-6C>G	XP_011535368.1:n.505-6C>G
XM_017021580.2:c.598-6C>G	XP_016877069.1:n.598-6C>G
XM_017021581.2:c.598-6C>G	XP_016877070.1:n.598-6C>G
XM_024449688.1:c.505-6C>G	XP_024305456.1:n.505-6C>G
XR_001750501.2:n.720-6C>G
NM_001193314.2:c.598-6C>G	NP_001180243.1:n.598-6C>G
NM_001193316.2:c.451-6C>G	NP_001180245.1:n.451-6C>G
NM_001193317.2:c.598-6C>G	NP_001180246.1:n.598-6C>G
NM_022067.4:c.598-6C>G	NP_071350.2:n.598-6C>G
NM_001193315.2:c.598-6C>G MANE Select	NP_001180244.1:n.598-6C>G
NM_001400324.1:c.451-6C>G	NP_001387253.1:n.451-6C>G
NM_001400325.1:c.451-6C>G	NP_001387254.1:n.451-6C>G
NM_001400326.1:c.598-6C>G	NP_001387255.1:n.598-6C>G
NM_001400327.1:c.565-6C>G	NP_001387256.1:n.565-6C>G
NM_001400330.1:c.598-6C>G	NP_001387259.1:n.598-6C>G
NM_001400331.1:c.598-6C>G	NP_001387260.1:n.598-6C>G
NM_001400332.1:c.598-6C>G	NP_001387261.1:n.598-6C>G
NM_001400333.1:c.505-6C>G	NP_001387262.1:n.505-6C>G
NM_001400334.1:c.505-6C>G	NP_001387263.1:n.505-6C>G
NM_001400335.1:c.598-6C>G	NP_001387264.1:n.598-6C>G
NM_001400336.1:c.598-6C>G	NP_001387265.1:n.598-6C>G
NM_001400337.1:c.358-6C>G	NP_001387266.1:n.358-6C>G
NM_001400338.1:c.598-6C>G	NP_001387267.1:n.598-6C>G
NM_001400339.1:c.598-6C>G	NP_001387268.1:n.598-6C>G
NR_174476.1:n.705-6C>G