Canonical Allele Identifier: CA390697177

Gene: VIPAS39

Linked Data

• MyVariant Identifiers: chr14:g.77901702G>C (hg19) ; chr14:g.77435359G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77435359G>C , CM000676.2:g.77435359G>C	GRCh38
NC_000014.8:g.77901702G>C , CM000676.1:g.77901702G>C	GRCh37
NC_000014.7:g.76971455G>C	NCBI36
NG_023421.1:g.27282C>G
NG_023421.2:g.27282C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557658.6:c.947C>G MANE Select	ENSP00000452191.1:p.Thr316Ser
ENST00000327028.8:c.800C>G	ENSP00000313098.5:p.Thr267Ser
ENST00000343765.6:c.947C>G	ENSP00000339122.2:p.Thr316Ser
ENST00000448935.6:c.800C>G	ENSP00000404815.2:p.Thr267Ser
ENST00000553576.5:n.359C>G
ENST00000553888.5:c.947C>G	ENSP00000452181.1:p.Thr316Ser
ENST00000556412.4:c.1025C>G	ENSP00000451857.1:p.Thr342Ser
ENST00000557658.5:c.947C>G	ENSP00000452191.1:p.Thr316Ser
NM_001193314.1:c.947C>G	NP_001180243.1:p.Thr316Ser
NM_001193315.1:c.947C>G	NP_001180244.1:p.Thr316Ser
NM_001193316.1:c.800C>G	NP_001180245.1:p.Thr267Ser
NM_001193317.1:c.947C>G	NP_001180246.1:p.Thr316Ser
NM_022067.3:c.947C>G	NP_071350.2:p.Thr316Ser
XM_011537066.1:c.854C>G	XP_011535368.1:p.Thr285Ser
XM_011537066.2:c.854C>G	XP_011535368.1:p.Thr285Ser
XM_017021580.2:c.947C>G	XP_016877069.1:p.Thr316Ser
XM_017021581.2:c.947C>G	XP_016877070.1:p.Thr316Ser
XM_024449688.1:c.854C>G	XP_024305456.1:p.Thr285Ser
XR_001750501.2:n.1069C>G
NM_001193314.2:c.947C>G	NP_001180243.1:p.Thr316Ser
NM_001193316.2:c.800C>G	NP_001180245.1:p.Thr267Ser
NM_001193317.2:c.947C>G	NP_001180246.1:p.Thr316Ser
NM_022067.4:c.947C>G	NP_071350.2:p.Thr316Ser
NM_001193315.2:c.947C>G MANE Select	NP_001180244.1:p.Thr316Ser
NM_001400324.1:c.800C>G	NP_001387253.1:p.Thr267Ser
NM_001400325.1:c.800C>G	NP_001387254.1:p.Thr267Ser
NM_001400326.1:c.947C>G	NP_001387255.1:p.Thr316Ser
NM_001400327.1:c.914C>G	NP_001387256.1:p.Thr305Ser
NM_001400330.1:c.947C>G	NP_001387259.1:p.Thr316Ser
NM_001400331.1:c.947C>G	NP_001387260.1:p.Thr316Ser
NM_001400332.1:c.947C>G	NP_001387261.1:p.Thr316Ser
NM_001400333.1:c.854C>G	NP_001387262.1:p.Thr285Ser
NM_001400334.1:c.854C>G	NP_001387263.1:p.Thr285Ser
NM_001400335.1:c.947C>G	NP_001387264.1:p.Thr316Ser
NM_001400336.1:c.912+485C>G	NP_001387265.1:n.912+485C>G
NM_001400337.1:c.707C>G	NP_001387266.1:p.Thr236Ser
NM_001400338.1:c.845C>G	NP_001387267.1:p.Thr282Ser
NM_001400339.1:c.763-1056C>G	NP_001387268.1:n.763-1056C>G
NR_174476.1:n.1054C>G