Canonical Allele Identifier: CA2573896639

Gene: PRUNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151017866del , CM000663.2:g.151017866del	GRCh38
NC_000001.10:g.150990342del , CM000663.1:g.150990342del	GRCh37
NC_000001.9:g.149256966del	NCBI36
NG_052875.1:g.14476del

Transcript Alleles

HGVS	Amino-acid change
ENST00000271620.8:c.94del MANE Select	ENSP00000271620.3:p.Thr32GlnfsTer11
ENST00000650332.1:c.94del	ENSP00000497847.1:p.Thr32GlnfsTer11
ENST00000271620.7:c.94del	ENSP00000271620.3:p.Thr32GlnfsTer11
ENST00000368935.1:c.-56del	ENSP00000357931.1:n.-56del
ENST00000368936.5:c.-250del	ENSP00000357932.1:n.-250del
ENST00000368937.5:c.-26-7649del	ENSP00000357933.1:n.-26-7649del
ENST00000431193.5:c.-65del	ENSP00000392632.1:n.-65del
ENST00000450884.5:c.-211-6745del	ENSP00000387696.1:n.-211-6745del
ENST00000462440.5:n.277del
ENST00000467771.5:n.307del
ENST00000475722.5:n.260del
NM_001303229.1:c.-250del	NP_001290158.1:n.-250del
NM_001303242.1:c.94del	NP_001290171.1:p.Thr32GlnfsTer11
NM_001303243.1:c.-166del	NP_001290172.1:n.-166del
NM_021222.2:c.94del	NP_067045.1:p.Thr32GlnfsTer11
NR_130130.1:n.282-7649del
NR_130131.1:n.336del
NR_130132.1:n.336del
NR_130135.1:n.336del
XM_005245393.3:c.94del	XP_005245450.1:p.Thr32GlnfsTer11
XM_005245397.3:c.-65del	XP_005245454.1:n.-65del
XM_011509830.1:c.94del	XP_011508132.1:p.Thr32GlnfsTer11
XM_011509831.1:c.-76del	XP_011508133.1:n.-76del
XM_011509832.1:c.-211-6745del	XP_011508134.1:n.-211-6745del
XM_005245393.5:c.94del	XP_005245450.1:p.Thr32GlnfsTer11
XM_011509832.2:c.-211-6745del	XP_011508134.1:n.-211-6745del
XM_017001955.2:c.94del	XP_016857444.1:p.Thr32GlnfsTer11
XM_017001956.1:c.-65del	XP_016857445.1:n.-65del
XM_017001957.1:c.-76del	XP_016857446.1:n.-76del
NM_021222.3:c.94del MANE Select	NP_067045.1:p.Thr32GlnfsTer11
NM_001303229.2:c.-250del	NP_001290158.1:n.-250del
NM_001303242.2:c.94del	NP_001290171.1:p.Thr32GlnfsTer11
NM_001303243.2:c.-166del	NP_001290172.1:n.-166del
NR_130130.2:n.224-7649del
NR_130131.2:n.278del
NR_130132.2:n.278del
NR_130135.2:n.278del