Canonical Allele Identifier: CA341902952
Gene: PRUNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151017870T>G , CM000663.2:g.151017870T>G GRCh38
NC_000001.10:g.150990346T>G , CM000663.1:g.150990346T>G GRCh37
NC_000001.9:g.149256970T>G NCBI36
NG_052875.1:g.14480T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000271620.8:c.98T>G MANE Select ENSP00000271620.3:p.Val33Gly
ENST00000650332.1:c.98T>G ENSP00000497847.1:p.Val33Gly
ENST00000271620.7:c.98T>G ENSP00000271620.3:p.Val33Gly
ENST00000368935.1:c.-52T>G ENSP00000357931.1:n.-52T>G
ENST00000368936.5:c.-246T>G ENSP00000357932.1:n.-246T>G
ENST00000368937.5:c.-26-7645T>G ENSP00000357933.1:n.-26-7645T>G
ENST00000431193.5:c.-61T>G ENSP00000392632.1:n.-61T>G
ENST00000450884.5:c.-211-6741T>G ENSP00000387696.1:n.-211-6741T>G
ENST00000462440.5:n.281T>G
ENST00000467771.5:n.311T>G
ENST00000475722.5:n.264T>G
NM_001303229.1:c.-246T>G NP_001290158.1:n.-246T>G
NM_001303242.1:c.98T>G NP_001290171.1:p.Val33Gly
NM_001303243.1:c.-162T>G NP_001290172.1:n.-162T>G
NM_021222.2:c.98T>G NP_067045.1:p.Val33Gly
NR_130130.1:n.282-7645T>G
NR_130131.1:n.340T>G
NR_130132.1:n.340T>G
NR_130135.1:n.340T>G
XM_005245393.3:c.98T>G XP_005245450.1:p.Val33Gly
XM_005245397.3:c.-61T>G XP_005245454.1:n.-61T>G
XM_011509830.1:c.98T>G XP_011508132.1:p.Val33Gly
XM_011509831.1:c.-72T>G XP_011508133.1:n.-72T>G
XM_011509832.1:c.-211-6741T>G XP_011508134.1:n.-211-6741T>G
XM_005245393.5:c.98T>G XP_005245450.1:p.Val33Gly
XM_011509832.2:c.-211-6741T>G XP_011508134.1:n.-211-6741T>G
XM_017001955.2:c.98T>G XP_016857444.1:p.Val33Gly
XM_017001956.1:c.-61T>G XP_016857445.1:n.-61T>G
XM_017001957.1:c.-72T>G XP_016857446.1:n.-72T>G
NM_021222.3:c.98T>G MANE Select NP_067045.1:p.Val33Gly
NM_001303229.2:c.-246T>G NP_001290158.1:n.-246T>G
NM_001303242.2:c.98T>G NP_001290171.1:p.Val33Gly
NM_001303243.2:c.-162T>G NP_001290172.1:n.-162T>G
NR_130130.2:n.224-7645T>G
NR_130131.2:n.282T>G
NR_130132.2:n.282T>G
NR_130135.2:n.282T>G