Canonical Allele Identifier: CA2479404383

Gene: PRUNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151017945_151017946delinsGA , CM000663.2:g.151017945_151017946delinsGA	GRCh38
NC_000001.10:g.150990421_150990422delinsGA , CM000663.1:g.150990421_150990422delinsGA	GRCh37
NC_000001.9:g.149257045_149257046delinsGA	NCBI36
NG_052875.1:g.14555_14556delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271620.8:c.132+41_132+42delinsGA MANE Select	ENSP00000271620.3:n.132+41_132+42delinsGA
ENST00000650332.1:c.132+41_132+42delinsGA	ENSP00000497847.1:n.132+41_132+42delinsGA
ENST00000271620.7:c.132+41_132+42delinsGA	ENSP00000271620.3:n.132+41_132+42delinsGA
ENST00000368935.1:c.-18+41_-18+42delinsGA	ENSP00000357931.1:n.-18+41_-18+42delinsGA
ENST00000368936.5:c.-212+41_-212+42delinsGA	ENSP00000357932.1:n.-212+41_-212+42delinsGA
ENST00000368937.5:c.-26-7570_-26-7569delinsGA	ENSP00000357933.1:n.-26-7570_-26-7569delinsGA
ENST00000431193.5:c.-27+41_-27+42delinsGA	ENSP00000392632.1:n.-27+41_-27+42delinsGA
ENST00000450884.5:c.-211-6666_-211-6665delinsGA	ENSP00000387696.1:n.-211-6666_-211-6665delinsGA
ENST00000462440.5:n.315+41_315+42delinsGA
ENST00000467771.5:n.345+41_345+42delinsGA
ENST00000475722.5:n.298+41_298+42delinsGA
NM_001303229.1:c.-212+41_-212+42delinsGA	NP_001290158.1:n.-212+41_-212+42delinsGA
NM_001303242.1:c.132+41_132+42delinsGA	NP_001290171.1:n.132+41_132+42delinsGA
NM_001303243.1:c.-128+41_-128+42delinsGA	NP_001290172.1:n.-128+41_-128+42delinsGA
NM_021222.2:c.132+41_132+42delinsGA	NP_067045.1:n.132+41_132+42delinsGA
NR_130130.1:n.282-7570_282-7569delinsGA
NR_130131.1:n.374+41_374+42delinsGA
NR_130132.1:n.374+41_374+42delinsGA
NR_130135.1:n.374+41_374+42delinsGA
XM_005245393.3:c.132+41_132+42delinsGA	XP_005245450.1:n.132+41_132+42delinsGA
XM_005245397.3:c.-27+41_-27+42delinsGA	XP_005245454.1:n.-27+41_-27+42delinsGA
XM_011509830.1:c.132+41_132+42delinsGA	XP_011508132.1:n.132+41_132+42delinsGA
XM_011509831.1:c.-38+41_-38+42delinsGA	XP_011508133.1:n.-38+41_-38+42delinsGA
XM_011509832.1:c.-211-6666_-211-6665delinsGA	XP_011508134.1:n.-211-6666_-211-6665delinsGA
XM_005245393.5:c.132+41_132+42delinsGA	XP_005245450.1:n.132+41_132+42delinsGA
XM_011509832.2:c.-211-6666_-211-6665delinsGA	XP_011508134.1:n.-211-6666_-211-6665delinsGA
XM_017001955.2:c.132+41_132+42delinsGA	XP_016857444.1:n.132+41_132+42delinsGA
XM_017001956.1:c.-27+41_-27+42delinsGA	XP_016857445.1:n.-27+41_-27+42delinsGA
XM_017001957.1:c.-38+41_-38+42delinsGA	XP_016857446.1:n.-38+41_-38+42delinsGA
NM_021222.3:c.132+41_132+42delinsGA MANE Select	NP_067045.1:n.132+41_132+42delinsGA
NM_001303229.2:c.-212+41_-212+42delinsGA	NP_001290158.1:n.-212+41_-212+42delinsGA
NM_001303242.2:c.132+41_132+42delinsGA	NP_001290171.1:n.132+41_132+42delinsGA
NM_001303243.2:c.-128+41_-128+42delinsGA	NP_001290172.1:n.-128+41_-128+42delinsGA
NR_130130.2:n.224-7570_224-7569delinsGA
NR_130131.2:n.316+41_316+42delinsGA
NR_130132.2:n.316+41_316+42delinsGA
NR_130135.2:n.316+41_316+42delinsGA