Canonical Allele Identifier: CA708742688

Gene: VIPAS39

Linked Data

• dbSNP Id: rs1342697791
• gnomAD v4: 14-77428284-C-A
• MyVariant Identifiers: chr14:g.77894627C>A (hg19) ; chr14:g.77428284C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77428284C>A , CM000676.2:g.77428284C>A	GRCh38
NC_000014.8:g.77894627C>A , CM000676.1:g.77894627C>A	GRCh37
NC_000014.7:g.76964380C>A	NCBI36
NG_023421.1:g.34357G>T
NG_023421.2:g.34357G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557658.6:c.1461+86G>T MANE Select	ENSP00000452191.1:n.1461+86G>T
ENST00000327028.8:c.1314+86G>T	ENSP00000313098.5:n.1314+86G>T
ENST00000343765.6:c.1461+86G>T	ENSP00000339122.2:n.1461+86G>T
ENST00000448935.6:c.1314+86G>T	ENSP00000404815.2:n.1314+86G>T
ENST00000553888.5:c.1461+86G>T	ENSP00000452181.1:n.1461+86G>T
ENST00000556412.4:c.1539+86G>T	ENSP00000451857.1:n.1539+86G>T
ENST00000557658.5:c.1461+86G>T	ENSP00000452191.1:n.1461+86G>T
NM_001193314.1:c.1461+86G>T	NP_001180243.1:n.1461+86G>T
NM_001193315.1:c.1461+86G>T	NP_001180244.1:n.1461+86G>T
NM_001193316.1:c.1314+86G>T	NP_001180245.1:n.1314+86G>T
NM_001193317.1:c.1461+86G>T	NP_001180246.1:n.1461+86G>T
NM_022067.3:c.1461+86G>T	NP_071350.2:n.1461+86G>T
XM_011537066.1:c.1368+86G>T	XP_011535368.1:n.1368+86G>T
XM_011537066.2:c.1368+86G>T	XP_011535368.1:n.1368+86G>T
XM_024449688.1:c.1368+86G>T	XP_024305456.1:n.1368+86G>T
XR_001750501.2:n.1676+86G>T
NM_001193314.2:c.1461+86G>T	NP_001180243.1:n.1461+86G>T
NM_001193316.2:c.1314+86G>T	NP_001180245.1:n.1314+86G>T
NM_001193317.2:c.1461+86G>T	NP_001180246.1:n.1461+86G>T
NM_022067.4:c.1461+86G>T	NP_071350.2:n.1461+86G>T
NM_001193315.2:c.1461+86G>T MANE Select	NP_001180244.1:n.1461+86G>T
NM_001400324.1:c.1314+86G>T	NP_001387253.1:n.1314+86G>T
NM_001400325.1:c.1314+86G>T	NP_001387254.1:n.1314+86G>T
NM_001400326.1:c.1461+86G>T	NP_001387255.1:n.1461+86G>T
NM_001400327.1:c.1428+86G>T	NP_001387256.1:n.1428+86G>T
NM_001400330.1:c.1374+86G>T	NP_001387259.1:n.1374+86G>T
NM_001400331.1:c.1374+86G>T	NP_001387260.1:n.1374+86G>T
NM_001400332.1:c.1374+86G>T	NP_001387261.1:n.1374+86G>T
NM_001400333.1:c.1368+86G>T	NP_001387262.1:n.1368+86G>T
NM_001400334.1:c.1368+86G>T	NP_001387263.1:n.1368+86G>T
NM_001400335.1:c.1357-648G>T	NP_001387264.1:n.1357-648G>T
NM_001400336.1:c.1326+86G>T	NP_001387265.1:n.1326+86G>T
NM_001400337.1:c.1221+86G>T	NP_001387266.1:n.1221+86G>T
NM_001400338.1:c.1182+86G>T	NP_001387267.1:n.1182+86G>T
NM_001400339.1:c.1176+86G>T	NP_001387268.1:n.1176+86G>T
NR_174476.1:n.1661+86G>T