Canonical Allele Identifier: CA7287952

Gene: VIPAS39

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77437804T>C , CM000676.2:g.77437804T>C	GRCh38
NC_000014.8:g.77904147T>C , CM000676.1:g.77904147T>C	GRCh37
NC_000014.7:g.76973900T>C	NCBI36
NG_023421.1:g.24837A>G
NG_023421.2:g.24837A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557658.6:c.836+4A>G MANE Select	ENSP00000452191.1:n.836+4A>G
ENST00000327028.8:c.689+4A>G	ENSP00000313098.5:n.689+4A>G
ENST00000343765.6:c.836+4A>G	ENSP00000339122.2:n.836+4A>G
ENST00000448935.6:c.689+4A>G	ENSP00000404815.2:n.689+4A>G
ENST00000553576.5:n.248+4A>G
ENST00000553888.5:c.836+4A>G	ENSP00000452181.1:n.836+4A>G
ENST00000556412.4:c.914+4A>G	ENSP00000451857.1:n.914+4A>G
ENST00000557658.5:c.836+4A>G	ENSP00000452191.1:n.836+4A>G
NM_001193314.1:c.836+4A>G	NP_001180243.1:n.836+4A>G
NM_001193315.1:c.836+4A>G	NP_001180244.1:n.836+4A>G
NM_001193316.1:c.689+4A>G	NP_001180245.1:n.689+4A>G
NM_001193317.1:c.836+4A>G	NP_001180246.1:n.836+4A>G
NM_022067.3:c.836+4A>G	NP_071350.2:n.836+4A>G
XM_011537066.1:c.743+4A>G	XP_011535368.1:n.743+4A>G
XM_011537066.2:c.743+4A>G	XP_011535368.1:n.743+4A>G
XM_017021580.2:c.836+4A>G	XP_016877069.1:n.836+4A>G
XM_017021581.2:c.836+4A>G	XP_016877070.1:n.836+4A>G
XM_024449688.1:c.743+4A>G	XP_024305456.1:n.743+4A>G
XR_001750501.2:n.958+4A>G
NM_001193314.2:c.836+4A>G	NP_001180243.1:n.836+4A>G
NM_001193316.2:c.689+4A>G	NP_001180245.1:n.689+4A>G
NM_001193317.2:c.836+4A>G	NP_001180246.1:n.836+4A>G
NM_022067.4:c.836+4A>G	NP_071350.2:n.836+4A>G
NM_001193315.2:c.836+4A>G MANE Select	NP_001180244.1:n.836+4A>G
NM_001400324.1:c.689+4A>G	NP_001387253.1:n.689+4A>G
NM_001400325.1:c.689+4A>G	NP_001387254.1:n.689+4A>G
NM_001400326.1:c.836+4A>G	NP_001387255.1:n.836+4A>G
NM_001400327.1:c.803+4A>G	NP_001387256.1:n.803+4A>G
NM_001400330.1:c.836+4A>G	NP_001387259.1:n.836+4A>G
NM_001400331.1:c.836+4A>G	NP_001387260.1:n.836+4A>G
NM_001400332.1:c.836+4A>G	NP_001387261.1:n.836+4A>G
NM_001400333.1:c.743+4A>G	NP_001387262.1:n.743+4A>G
NM_001400334.1:c.743+4A>G	NP_001387263.1:n.743+4A>G
NM_001400335.1:c.836+4A>G	NP_001387264.1:n.836+4A>G
NM_001400336.1:c.836+4A>G	NP_001387265.1:n.836+4A>G
NM_001400337.1:c.596+4A>G	NP_001387266.1:n.596+4A>G
NM_001400338.1:c.735-1885A>G	NP_001387267.1:n.735-1885A>G
NM_001400339.1:c.762+3262A>G	NP_001387268.1:n.762+3262A>G
NR_174476.1:n.943+4A>G