Canonical Allele Identifier: CA2479404592
Gene: PRUNE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151018494C= , CM000663.2:g.151018494C= GRCh38
NC_000001.10:g.150990970C= , CM000663.1:g.150990970C= GRCh37
NC_000001.9:g.149257594C= NCBI36
NG_052875.1:g.15104C=

Transcript Alleles

HGVS Amino-acid change
ENST00000271620.8:c.160C= MANE Select ENSP00000271620.3:p.Pro54=
ENST00000650332.1:c.133-63C= ENSP00000497847.1:n.133-63C=
ENST00000271620.7:c.160C= ENSP00000271620.3:p.Pro54=
ENST00000368935.1:c.-18+590C= ENSP00000357931.1:n.-18+590C=
ENST00000368936.5:c.-212+590C= ENSP00000357932.1:n.-212+590C=
ENST00000368937.5:c.-26-7021C= ENSP00000357933.1:n.-26-7021C=
ENST00000431193.5:c.-27+590C= ENSP00000392632.1:n.-27+590C=
ENST00000450884.5:c.-211-6117C= ENSP00000387696.1:n.-211-6117C=
ENST00000462440.5:n.316-63C=
ENST00000467771.5:n.346-63C=
ENST00000475722.5:n.326C=
NM_001303229.1:c.-212+590C= NP_001290158.1:n.-212+590C=
NM_001303242.1:c.160C= NP_001290171.1:p.Pro54=
NM_001303243.1:c.-100C= NP_001290172.1:n.-100C=
NM_021222.2:c.160C= NP_067045.1:p.Pro54=
NR_130130.1:n.282-7021C=
NR_130131.1:n.374+590C=
NR_130132.1:n.374+590C=
NR_130135.1:n.374+590C=
XM_005245393.3:c.133-63C= XP_005245450.1:n.133-63C=
XM_005245397.3:c.-27+590C= XP_005245454.1:n.-27+590C=
XM_011509830.1:c.160C= XP_011508132.1:p.Pro54=
XM_011509831.1:c.-37-63C= XP_011508133.1:n.-37-63C=
XM_011509832.1:c.-211-6117C= XP_011508134.1:n.-211-6117C=
XM_005245393.5:c.133-63C= XP_005245450.1:n.133-63C=
XM_011509832.2:c.-211-6117C= XP_011508134.1:n.-211-6117C=
XM_017001955.2:c.133-63C= XP_016857444.1:n.133-63C=
XM_017001956.1:c.-27+590C= XP_016857445.1:n.-27+590C=
XM_017001957.1:c.-37-63C= XP_016857446.1:n.-37-63C=
NM_021222.3:c.160C= MANE Select NP_067045.1:p.Pro54=
NM_001303229.2:c.-212+590C= NP_001290158.1:n.-212+590C=
NM_001303242.2:c.160C= NP_001290171.1:p.Pro54=
NM_001303243.2:c.-100C= NP_001290172.1:n.-100C=
NR_130130.2:n.224-7021C=
NR_130131.2:n.316+590C=
NR_130132.2:n.316+590C=
NR_130135.2:n.316+590C=