Canonical Allele Identifier: CA2746092376

Gene: PRUNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151017911_151017917dup , CM000663.2:g.151017911_151017917dup	GRCh38
NC_000001.10:g.150990387_150990393dup , CM000663.1:g.150990387_150990393dup	GRCh37
NC_000001.9:g.149257011_149257017dup	NCBI36
NG_052875.1:g.14521_14527dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271620.8:c.132+7_132+13dup MANE Select	ENSP00000271620.3:n.132+7_132+13dup
ENST00000650332.1:c.132+7_132+13dup	ENSP00000497847.1:n.132+7_132+13dup
ENST00000271620.7:c.132+7_132+13dup	ENSP00000271620.3:n.132+7_132+13dup
ENST00000368935.1:c.-18+7_-18+13dup	ENSP00000357931.1:n.-18+7_-18+13dup
ENST00000368936.5:c.-212+7_-212+13dup	ENSP00000357932.1:n.-212+7_-212+13dup
ENST00000368937.5:c.-26-7604_-26-7598dup	ENSP00000357933.1:n.-26-7604_-26-7598dup
ENST00000431193.5:c.-27+7_-27+13dup	ENSP00000392632.1:n.-27+7_-27+13dup
ENST00000450884.5:c.-211-6700_-211-6694dup	ENSP00000387696.1:n.-211-6700_-211-6694dup
ENST00000462440.5:n.315+7_315+13dup
ENST00000467771.5:n.345+7_345+13dup
ENST00000475722.5:n.298+7_298+13dup
NM_001303229.1:c.-212+7_-212+13dup	NP_001290158.1:n.-212+7_-212+13dup
NM_001303242.1:c.132+7_132+13dup	NP_001290171.1:n.132+7_132+13dup
NM_001303243.1:c.-128+7_-128+13dup	NP_001290172.1:n.-128+7_-128+13dup
NM_021222.2:c.132+7_132+13dup	NP_067045.1:n.132+7_132+13dup
NR_130130.1:n.282-7604_282-7598dup
NR_130131.1:n.374+7_374+13dup
NR_130132.1:n.374+7_374+13dup
NR_130135.1:n.374+7_374+13dup
XM_005245393.3:c.132+7_132+13dup	XP_005245450.1:n.132+7_132+13dup
XM_005245397.3:c.-27+7_-27+13dup	XP_005245454.1:n.-27+7_-27+13dup
XM_011509830.1:c.132+7_132+13dup	XP_011508132.1:n.132+7_132+13dup
XM_011509831.1:c.-38+7_-38+13dup	XP_011508133.1:n.-38+7_-38+13dup
XM_011509832.1:c.-211-6700_-211-6694dup	XP_011508134.1:n.-211-6700_-211-6694dup
XM_005245393.5:c.132+7_132+13dup	XP_005245450.1:n.132+7_132+13dup
XM_011509832.2:c.-211-6700_-211-6694dup	XP_011508134.1:n.-211-6700_-211-6694dup
XM_017001955.2:c.132+7_132+13dup	XP_016857444.1:n.132+7_132+13dup
XM_017001956.1:c.-27+7_-27+13dup	XP_016857445.1:n.-27+7_-27+13dup
XM_017001957.1:c.-38+7_-38+13dup	XP_016857446.1:n.-38+7_-38+13dup
NM_021222.3:c.132+7_132+13dup MANE Select	NP_067045.1:n.132+7_132+13dup
NM_001303229.2:c.-212+7_-212+13dup	NP_001290158.1:n.-212+7_-212+13dup
NM_001303242.2:c.132+7_132+13dup	NP_001290171.1:n.132+7_132+13dup
NM_001303243.2:c.-128+7_-128+13dup	NP_001290172.1:n.-128+7_-128+13dup
NR_130130.2:n.224-7604_224-7598dup
NR_130131.2:n.316+7_316+13dup
NR_130132.2:n.316+7_316+13dup
NR_130135.2:n.316+7_316+13dup