Canonical Allele Identifier: CA341902916
Gene: PRUNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151017861A>C , CM000663.2:g.151017861A>C GRCh38
NC_000001.10:g.150990337A>C , CM000663.1:g.150990337A>C GRCh37
NC_000001.9:g.149256961A>C NCBI36
NG_052875.1:g.14471A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271620.8:c.89A>C MANE Select ENSP00000271620.3:p.Asp30Ala
ENST00000650332.1:c.89A>C ENSP00000497847.1:p.Asp30Ala
ENST00000271620.7:c.89A>C ENSP00000271620.3:p.Asp30Ala
ENST00000368935.1:c.-61A>C ENSP00000357931.1:n.-61A>C
ENST00000368936.5:c.-255A>C ENSP00000357932.1:n.-255A>C
ENST00000368937.5:c.-26-7654A>C ENSP00000357933.1:n.-26-7654A>C
ENST00000431193.5:c.-70A>C ENSP00000392632.1:n.-70A>C
ENST00000450884.5:c.-211-6750A>C ENSP00000387696.1:n.-211-6750A>C
ENST00000462440.5:n.272A>C
ENST00000467771.5:n.302A>C
ENST00000475722.5:n.255A>C
NM_001303229.1:c.-255A>C NP_001290158.1:n.-255A>C
NM_001303242.1:c.89A>C NP_001290171.1:p.Asp30Ala
NM_001303243.1:c.-171A>C NP_001290172.1:n.-171A>C
NM_021222.2:c.89A>C NP_067045.1:p.Asp30Ala
NR_130130.1:n.282-7654A>C
NR_130131.1:n.331A>C
NR_130132.1:n.331A>C
NR_130135.1:n.331A>C
XM_005245393.3:c.89A>C XP_005245450.1:p.Asp30Ala
XM_005245397.3:c.-70A>C XP_005245454.1:n.-70A>C
XM_011509830.1:c.89A>C XP_011508132.1:p.Asp30Ala
XM_011509831.1:c.-81A>C XP_011508133.1:n.-81A>C
XM_011509832.1:c.-211-6750A>C XP_011508134.1:n.-211-6750A>C
XM_005245393.5:c.89A>C XP_005245450.1:p.Asp30Ala
XM_011509832.2:c.-211-6750A>C XP_011508134.1:n.-211-6750A>C
XM_017001955.2:c.89A>C XP_016857444.1:p.Asp30Ala
XM_017001956.1:c.-70A>C XP_016857445.1:n.-70A>C
XM_017001957.1:c.-81A>C XP_016857446.1:n.-81A>C
NM_021222.3:c.89A>C MANE Select NP_067045.1:p.Asp30Ala
NM_001303229.2:c.-255A>C NP_001290158.1:n.-255A>C
NM_001303242.2:c.89A>C NP_001290171.1:p.Asp30Ala
NM_001303243.2:c.-171A>C NP_001290172.1:n.-171A>C
NR_130130.2:n.224-7654A>C
NR_130131.2:n.273A>C
NR_130132.2:n.273A>C
NR_130135.2:n.273A>C