Canonical Allele Identifier: CA390697158

Gene: VIPAS39

Linked Data

• MyVariant Identifiers: chr14:g.77901694A>C (hg19) ; chr14:g.77435351A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77435351A>C , CM000676.2:g.77435351A>C	GRCh38
NC_000014.8:g.77901694A>C , CM000676.1:g.77901694A>C	GRCh37
NC_000014.7:g.76971447A>C	NCBI36
NG_023421.1:g.27290T>G
NG_023421.2:g.27290T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557658.6:c.955T>G MANE Select	ENSP00000452191.1:p.Phe319Val
ENST00000327028.8:c.808T>G	ENSP00000313098.5:p.Phe270Val
ENST00000343765.6:c.955T>G	ENSP00000339122.2:p.Phe319Val
ENST00000448935.6:c.808T>G	ENSP00000404815.2:p.Phe270Val
ENST00000553576.5:n.367T>G
ENST00000553888.5:c.955T>G	ENSP00000452181.1:p.Phe319Val
ENST00000556412.4:c.1033T>G	ENSP00000451857.1:p.Phe345Val
ENST00000557658.5:c.955T>G	ENSP00000452191.1:p.Phe319Val
NM_001193314.1:c.955T>G	NP_001180243.1:p.Phe319Val
NM_001193315.1:c.955T>G	NP_001180244.1:p.Phe319Val
NM_001193316.1:c.808T>G	NP_001180245.1:p.Phe270Val
NM_001193317.1:c.955T>G	NP_001180246.1:p.Phe319Val
NM_022067.3:c.955T>G	NP_071350.2:p.Phe319Val
XM_011537066.1:c.862T>G	XP_011535368.1:p.Phe288Val
XM_011537066.2:c.862T>G	XP_011535368.1:p.Phe288Val
XM_017021580.2:c.955T>G	XP_016877069.1:p.Phe319Val
XM_017021581.2:c.955T>G	XP_016877070.1:p.Phe319Val
XM_024449688.1:c.862T>G	XP_024305456.1:p.Phe288Val
XR_001750501.2:n.1077T>G
NM_001193314.2:c.955T>G	NP_001180243.1:p.Phe319Val
NM_001193316.2:c.808T>G	NP_001180245.1:p.Phe270Val
NM_001193317.2:c.955T>G	NP_001180246.1:p.Phe319Val
NM_022067.4:c.955T>G	NP_071350.2:p.Phe319Val
NM_001193315.2:c.955T>G MANE Select	NP_001180244.1:p.Phe319Val
NM_001400324.1:c.808T>G	NP_001387253.1:p.Phe270Val
NM_001400325.1:c.808T>G	NP_001387254.1:p.Phe270Val
NM_001400326.1:c.955T>G	NP_001387255.1:p.Phe319Val
NM_001400327.1:c.922T>G	NP_001387256.1:p.Phe308Val
NM_001400330.1:c.955T>G	NP_001387259.1:p.Phe319Val
NM_001400331.1:c.955T>G	NP_001387260.1:p.Phe319Val
NM_001400332.1:c.955T>G	NP_001387261.1:p.Phe319Val
NM_001400333.1:c.862T>G	NP_001387262.1:p.Phe288Val
NM_001400334.1:c.862T>G	NP_001387263.1:p.Phe288Val
NM_001400335.1:c.955T>G	NP_001387264.1:p.Phe319Val
NM_001400336.1:c.912+493T>G	NP_001387265.1:n.912+493T>G
NM_001400337.1:c.715T>G	NP_001387266.1:p.Phe239Val
NM_001400338.1:c.853T>G	NP_001387267.1:p.Phe285Val
NM_001400339.1:c.763-1048T>G	NP_001387268.1:n.763-1048T>G
NR_174476.1:n.1062T>G