Canonical Allele Identifier: CA341902945
Gene: PRUNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151017869G>A , CM000663.2:g.151017869G>A GRCh38
NC_000001.10:g.150990345G>A , CM000663.1:g.150990345G>A GRCh37
NC_000001.9:g.149256969G>A NCBI36
NG_052875.1:g.14479G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000271620.8:c.97G>A MANE Select ENSP00000271620.3:p.Val33Met
ENST00000650332.1:c.97G>A ENSP00000497847.1:p.Val33Met
ENST00000271620.7:c.97G>A ENSP00000271620.3:p.Val33Met
ENST00000368935.1:c.-53G>A ENSP00000357931.1:n.-53G>A
ENST00000368936.5:c.-247G>A ENSP00000357932.1:n.-247G>A
ENST00000368937.5:c.-26-7646G>A ENSP00000357933.1:n.-26-7646G>A
ENST00000431193.5:c.-62G>A ENSP00000392632.1:n.-62G>A
ENST00000450884.5:c.-211-6742G>A ENSP00000387696.1:n.-211-6742G>A
ENST00000462440.5:n.280G>A
ENST00000467771.5:n.310G>A
ENST00000475722.5:n.263G>A
NM_001303229.1:c.-247G>A NP_001290158.1:n.-247G>A
NM_001303242.1:c.97G>A NP_001290171.1:p.Val33Met
NM_001303243.1:c.-163G>A NP_001290172.1:n.-163G>A
NM_021222.2:c.97G>A NP_067045.1:p.Val33Met
NR_130130.1:n.282-7646G>A
NR_130131.1:n.339G>A
NR_130132.1:n.339G>A
NR_130135.1:n.339G>A
XM_005245393.3:c.97G>A XP_005245450.1:p.Val33Met
XM_005245397.3:c.-62G>A XP_005245454.1:n.-62G>A
XM_011509830.1:c.97G>A XP_011508132.1:p.Val33Met
XM_011509831.1:c.-73G>A XP_011508133.1:n.-73G>A
XM_011509832.1:c.-211-6742G>A XP_011508134.1:n.-211-6742G>A
XM_005245393.5:c.97G>A XP_005245450.1:p.Val33Met
XM_011509832.2:c.-211-6742G>A XP_011508134.1:n.-211-6742G>A
XM_017001955.2:c.97G>A XP_016857444.1:p.Val33Met
XM_017001956.1:c.-62G>A XP_016857445.1:n.-62G>A
XM_017001957.1:c.-73G>A XP_016857446.1:n.-73G>A
NM_021222.3:c.97G>A MANE Select NP_067045.1:p.Val33Met
NM_001303229.2:c.-247G>A NP_001290158.1:n.-247G>A
NM_001303242.2:c.97G>A NP_001290171.1:p.Val33Met
NM_001303243.2:c.-163G>A NP_001290172.1:n.-163G>A
NR_130130.2:n.224-7646G>A
NR_130131.2:n.281G>A
NR_130132.2:n.281G>A
NR_130135.2:n.281G>A