Canonical Allele Identifier: CA2479404560

Gene: PRUNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151018398_151018399delinsCA , CM000663.2:g.151018398_151018399delinsCA	GRCh38
NC_000001.10:g.150990874_150990875delinsCA , CM000663.1:g.150990874_150990875delinsCA	GRCh37
NC_000001.9:g.149257498_149257499delinsCA	NCBI36
NG_052875.1:g.15008_15009delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000271620.8:c.133-69_133-68delinsCA MANE Select	ENSP00000271620.3:n.133-69_133-68delinsCA
ENST00000650332.1:c.133-159_133-158delinsCA	ENSP00000497847.1:n.133-159_133-158delinsCA
ENST00000271620.7:c.133-69_133-68delinsCA	ENSP00000271620.3:n.133-69_133-68delinsCA
ENST00000368935.1:c.-18+494_-18+495delinsCA	ENSP00000357931.1:n.-18+494_-18+495delinsCA
ENST00000368936.5:c.-212+494_-212+495delinsCA	ENSP00000357932.1:n.-212+494_-212+495delinsCA
ENST00000368937.5:c.-26-7117_-26-7116delinsCA	ENSP00000357933.1:n.-26-7117_-26-7116delinsCA
ENST00000431193.5:c.-27+494_-27+495delinsCA	ENSP00000392632.1:n.-27+494_-27+495delinsCA
ENST00000450884.5:c.-211-6213_-211-6212delinsCA	ENSP00000387696.1:n.-211-6213_-211-6212delinsCA
ENST00000462440.5:n.316-159_316-158delinsCA
ENST00000467771.5:n.346-159_346-158delinsCA
ENST00000475722.5:n.299-69_299-68delinsCA
NM_001303229.1:c.-212+494_-212+495delinsCA	NP_001290158.1:n.-212+494_-212+495delinsCA
NM_001303242.1:c.133-69_133-68delinsCA	NP_001290171.1:n.133-69_133-68delinsCA
NM_001303243.1:c.-127-69_-127-68delinsCA	NP_001290172.1:n.-127-69_-127-68delinsCA
NM_021222.2:c.133-69_133-68delinsCA	NP_067045.1:n.133-69_133-68delinsCA
NR_130130.1:n.282-7117_282-7116delinsCA
NR_130131.1:n.374+494_374+495delinsCA
NR_130132.1:n.374+494_374+495delinsCA
NR_130135.1:n.374+494_374+495delinsCA
XM_005245393.3:c.133-159_133-158delinsCA	XP_005245450.1:n.133-159_133-158delinsCA
XM_005245397.3:c.-27+494_-27+495delinsCA	XP_005245454.1:n.-27+494_-27+495delinsCA
XM_011509830.1:c.133-69_133-68delinsCA	XP_011508132.1:n.133-69_133-68delinsCA
XM_011509831.1:c.-37-159_-37-158delinsCA	XP_011508133.1:n.-37-159_-37-158delinsCA
XM_011509832.1:c.-211-6213_-211-6212delinsCA	XP_011508134.1:n.-211-6213_-211-6212delinsCA
XM_005245393.5:c.133-159_133-158delinsCA	XP_005245450.1:n.133-159_133-158delinsCA
XM_011509832.2:c.-211-6213_-211-6212delinsCA	XP_011508134.1:n.-211-6213_-211-6212delinsCA
XM_017001955.2:c.133-159_133-158delinsCA	XP_016857444.1:n.133-159_133-158delinsCA
XM_017001956.1:c.-27+494_-27+495delinsCA	XP_016857445.1:n.-27+494_-27+495delinsCA
XM_017001957.1:c.-37-159_-37-158delinsCA	XP_016857446.1:n.-37-159_-37-158delinsCA
NM_021222.3:c.133-69_133-68delinsCA MANE Select	NP_067045.1:n.133-69_133-68delinsCA
NM_001303229.2:c.-212+494_-212+495delinsCA	NP_001290158.1:n.-212+494_-212+495delinsCA
NM_001303242.2:c.133-69_133-68delinsCA	NP_001290171.1:n.133-69_133-68delinsCA
NM_001303243.2:c.-127-69_-127-68delinsCA	NP_001290172.1:n.-127-69_-127-68delinsCA
NR_130130.2:n.224-7117_224-7116delinsCA
NR_130131.2:n.316+494_316+495delinsCA
NR_130132.2:n.316+494_316+495delinsCA
NR_130135.2:n.316+494_316+495delinsCA