Canonical Allele Identifier: CA113864

Gene: VIPAS39

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77442636G>A , CM000676.2:g.77442636G>A	GRCh38
NC_000014.8:g.77908979G>A , CM000676.1:g.77908979G>A	GRCh37
NC_000014.7:g.76978732G>A	NCBI36
NG_023421.1:g.20005C>T
NG_023421.2:g.20005C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001193315.2:c.658C>T MANE Select	NP_001180244.1:p.Arg220Ter
ENST00000557658.6:c.658C>T MANE Select	ENSP00000452191.1:p.Arg220Ter
NM_001193314.1:c.658C>T	NP_001180243.1:p.Arg220Ter
NM_001193314.2:c.658C>T	NP_001180243.1:p.Arg220Ter
NM_001193315.1:c.658C>T	NP_001180244.1:p.Arg220Ter
NM_001193316.1:c.511C>T	NP_001180245.1:p.Arg171Ter
NM_001193316.2:c.511C>T	NP_001180245.1:p.Arg171Ter
NM_001193317.1:c.658C>T	NP_001180246.1:p.Arg220Ter
NM_001193317.2:c.658C>T	NP_001180246.1:p.Arg220Ter
NM_001400324.1:c.511C>T	NP_001387253.1:p.Arg171Ter
NM_001400325.1:c.511C>T	NP_001387254.1:p.Arg171Ter
NM_001400326.1:c.658C>T	NP_001387255.1:p.Arg220Ter
NM_001400327.1:c.625C>T	NP_001387256.1:p.Arg209Ter
NM_001400330.1:c.658C>T	NP_001387259.1:p.Arg220Ter
NM_001400331.1:c.658C>T	NP_001387260.1:p.Arg220Ter
NM_001400332.1:c.658C>T	NP_001387261.1:p.Arg220Ter
NM_001400333.1:c.565C>T	NP_001387262.1:p.Arg189Ter
NM_001400334.1:c.565C>T	NP_001387263.1:p.Arg189Ter
NM_001400335.1:c.658C>T	NP_001387264.1:p.Arg220Ter
NM_001400336.1:c.658C>T	NP_001387265.1:p.Arg220Ter
NM_001400337.1:c.418C>T	NP_001387266.1:p.Arg140Ter
NM_001400338.1:c.658C>T	NP_001387267.1:p.Arg220Ter
NM_001400339.1:c.658C>T	NP_001387268.1:p.Arg220Ter
NM_022067.3:c.658C>T	NP_071350.2:p.Arg220Ter
NM_022067.4:c.658C>T	NP_071350.2:p.Arg220Ter
NR_174476.1:n.765C>T
ENST00000327028.8:c.511C>T	ENSP00000313098.5:p.Arg171Ter
ENST00000343765.6:c.658C>T	ENSP00000339122.2:p.Arg220Ter
ENST00000448935.6:c.511C>T	ENSP00000404815.2:p.Arg171Ter
ENST00000553576.5:n.70C>T
ENST00000553691.5:n.548C>T
ENST00000553888.5:c.658C>T	ENSP00000452181.1:p.Arg220Ter
ENST00000555854.1:n.103C>T
ENST00000556412.4:c.736C>T	ENSP00000451857.1:p.Arg246Ter
ENST00000557658.5:c.658C>T	ENSP00000452191.1:p.Arg220Ter
XM_011537066.1:c.565C>T	XP_011535368.1:p.Arg189Ter
XM_011537066.2:c.565C>T	XP_011535368.1:p.Arg189Ter
XM_017021580.2:c.658C>T	XP_016877069.1:p.Arg220Ter
XM_017021581.2:c.658C>T	XP_016877070.1:p.Arg220Ter
XM_024449688.1:c.565C>T	XP_024305456.1:p.Arg189Ter
XR_001750501.2:n.780C>T