Canonical Allele Identifier: CA390697164

Gene: VIPAS39

Linked Data

• MyVariant Identifiers: chr14:g.77901696A>C (hg19) ; chr14:g.77435353A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77435353A>C , CM000676.2:g.77435353A>C	GRCh38
NC_000014.8:g.77901696A>C , CM000676.1:g.77901696A>C	GRCh37
NC_000014.7:g.76971449A>C	NCBI36
NG_023421.1:g.27288T>G
NG_023421.2:g.27288T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557658.6:c.953T>G MANE Select	ENSP00000452191.1:p.Ile318Ser
ENST00000327028.8:c.806T>G	ENSP00000313098.5:p.Ile269Ser
ENST00000343765.6:c.953T>G	ENSP00000339122.2:p.Ile318Ser
ENST00000448935.6:c.806T>G	ENSP00000404815.2:p.Ile269Ser
ENST00000553576.5:n.365T>G
ENST00000553888.5:c.953T>G	ENSP00000452181.1:p.Ile318Ser
ENST00000556412.4:c.1031T>G	ENSP00000451857.1:p.Ile344Ser
ENST00000557658.5:c.953T>G	ENSP00000452191.1:p.Ile318Ser
NM_001193314.1:c.953T>G	NP_001180243.1:p.Ile318Ser
NM_001193315.1:c.953T>G	NP_001180244.1:p.Ile318Ser
NM_001193316.1:c.806T>G	NP_001180245.1:p.Ile269Ser
NM_001193317.1:c.953T>G	NP_001180246.1:p.Ile318Ser
NM_022067.3:c.953T>G	NP_071350.2:p.Ile318Ser
XM_011537066.1:c.860T>G	XP_011535368.1:p.Ile287Ser
XM_011537066.2:c.860T>G	XP_011535368.1:p.Ile287Ser
XM_017021580.2:c.953T>G	XP_016877069.1:p.Ile318Ser
XM_017021581.2:c.953T>G	XP_016877070.1:p.Ile318Ser
XM_024449688.1:c.860T>G	XP_024305456.1:p.Ile287Ser
XR_001750501.2:n.1075T>G
NM_001193314.2:c.953T>G	NP_001180243.1:p.Ile318Ser
NM_001193316.2:c.806T>G	NP_001180245.1:p.Ile269Ser
NM_001193317.2:c.953T>G	NP_001180246.1:p.Ile318Ser
NM_022067.4:c.953T>G	NP_071350.2:p.Ile318Ser
NM_001193315.2:c.953T>G MANE Select	NP_001180244.1:p.Ile318Ser
NM_001400324.1:c.806T>G	NP_001387253.1:p.Ile269Ser
NM_001400325.1:c.806T>G	NP_001387254.1:p.Ile269Ser
NM_001400326.1:c.953T>G	NP_001387255.1:p.Ile318Ser
NM_001400327.1:c.920T>G	NP_001387256.1:p.Ile307Ser
NM_001400330.1:c.953T>G	NP_001387259.1:p.Ile318Ser
NM_001400331.1:c.953T>G	NP_001387260.1:p.Ile318Ser
NM_001400332.1:c.953T>G	NP_001387261.1:p.Ile318Ser
NM_001400333.1:c.860T>G	NP_001387262.1:p.Ile287Ser
NM_001400334.1:c.860T>G	NP_001387263.1:p.Ile287Ser
NM_001400335.1:c.953T>G	NP_001387264.1:p.Ile318Ser
NM_001400336.1:c.912+491T>G	NP_001387265.1:n.912+491T>G
NM_001400337.1:c.713T>G	NP_001387266.1:p.Ile238Ser
NM_001400338.1:c.851T>G	NP_001387267.1:p.Ile284Ser
NM_001400339.1:c.763-1050T>G	NP_001387268.1:n.763-1050T>G
NR_174476.1:n.1060T>G