Canonical Allele Identifier: CA7287782

Gene: VIPAS39

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77429676A>G , CM000676.2:g.77429676A>G	GRCh38
NC_000014.8:g.77896019A>G , CM000676.1:g.77896019A>G	GRCh37
NC_000014.7:g.76965772A>G	NCBI36
NG_023421.1:g.32965T>C
NG_023421.2:g.32965T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557658.6:c.1266+5T>C MANE Select	ENSP00000452191.1:n.1266+5T>C
ENST00000327028.8:c.1119+5T>C	ENSP00000313098.5:n.1119+5T>C
ENST00000343765.6:c.1266+5T>C	ENSP00000339122.2:n.1266+5T>C
ENST00000448935.6:c.1119+5T>C	ENSP00000404815.2:n.1119+5T>C
ENST00000553888.5:c.1266+5T>C	ENSP00000452181.1:n.1266+5T>C
ENST00000556412.4:c.1344+5T>C	ENSP00000451857.1:n.1344+5T>C
ENST00000557658.5:c.1266+5T>C	ENSP00000452191.1:n.1266+5T>C
NM_001193314.1:c.1266+5T>C	NP_001180243.1:n.1266+5T>C
NM_001193315.1:c.1266+5T>C	NP_001180244.1:n.1266+5T>C
NM_001193316.1:c.1119+5T>C	NP_001180245.1:n.1119+5T>C
NM_001193317.1:c.1266+5T>C	NP_001180246.1:n.1266+5T>C
NM_022067.3:c.1266+5T>C	NP_071350.2:n.1266+5T>C
XM_011537066.1:c.1173+5T>C	XP_011535368.1:n.1173+5T>C
XM_011537066.2:c.1173+5T>C	XP_011535368.1:n.1173+5T>C
XM_024449688.1:c.1173+5T>C	XP_024305456.1:n.1173+5T>C
XR_001750501.2:n.1481+5T>C
NM_001193314.2:c.1266+5T>C	NP_001180243.1:n.1266+5T>C
NM_001193316.2:c.1119+5T>C	NP_001180245.1:n.1119+5T>C
NM_001193317.2:c.1266+5T>C	NP_001180246.1:n.1266+5T>C
NM_022067.4:c.1266+5T>C	NP_071350.2:n.1266+5T>C
NM_001193315.2:c.1266+5T>C MANE Select	NP_001180244.1:n.1266+5T>C
NM_001400324.1:c.1119+5T>C	NP_001387253.1:n.1119+5T>C
NM_001400325.1:c.1119+5T>C	NP_001387254.1:n.1119+5T>C
NM_001400326.1:c.1266+5T>C	NP_001387255.1:n.1266+5T>C
NM_001400327.1:c.1233+5T>C	NP_001387256.1:n.1233+5T>C
NM_001400330.1:c.1180-581T>C	NP_001387259.1:n.1180-581T>C
NM_001400331.1:c.1180-581T>C	NP_001387260.1:n.1180-581T>C
NM_001400332.1:c.1180-581T>C	NP_001387261.1:n.1180-581T>C
NM_001400333.1:c.1173+5T>C	NP_001387262.1:n.1173+5T>C
NM_001400334.1:c.1173+5T>C	NP_001387263.1:n.1173+5T>C
NM_001400335.1:c.1266+5T>C	NP_001387264.1:n.1266+5T>C
NM_001400336.1:c.1131+5T>C	NP_001387265.1:n.1131+5T>C
NM_001400337.1:c.1026+5T>C	NP_001387266.1:n.1026+5T>C
NM_001400338.1:c.988-581T>C	NP_001387267.1:n.988-581T>C
NM_001400339.1:c.981+5T>C	NP_001387268.1:n.981+5T>C
NR_174476.1:n.1466+5T>C