Canonical Allele Identifier: CA2479404355

Gene: PRUNE1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000271620.8:c.89A= MANE Select	ENSP00000271620.3:p.Asp30=
ENST00000650332.1:c.89A=	ENSP00000497847.1:p.Asp30=
ENST00000271620.7:c.89A=	ENSP00000271620.3:p.Asp30=
ENST00000368935.1:c.-61A=	ENSP00000357931.1:n.-61A=
ENST00000368936.5:c.-255A=	ENSP00000357932.1:n.-255A=
ENST00000368937.5:c.-26-7654A=	ENSP00000357933.1:n.-26-7654A=
ENST00000431193.5:c.-70A=	ENSP00000392632.1:n.-70A=
ENST00000450884.5:c.-211-6750A=	ENSP00000387696.1:n.-211-6750A=
ENST00000462440.5:n.272A=
ENST00000467771.5:n.302A=
ENST00000475722.5:n.255A=
NM_001303229.1:c.-255A=	NP_001290158.1:n.-255A=
NM_001303242.1:c.89A=	NP_001290171.1:p.Asp30=
NM_001303243.1:c.-171A=	NP_001290172.1:n.-171A=
NM_021222.2:c.89A=	NP_067045.1:p.Asp30=
NR_130130.1:n.282-7654A=
NR_130131.1:n.331A=
NR_130132.1:n.331A=
NR_130135.1:n.331A=
XM_005245393.3:c.89A=	XP_005245450.1:p.Asp30=
XM_005245397.3:c.-70A=	XP_005245454.1:n.-70A=
XM_011509830.1:c.89A=	XP_011508132.1:p.Asp30=
XM_011509831.1:c.-81A=	XP_011508133.1:n.-81A=
XM_011509832.1:c.-211-6750A=	XP_011508134.1:n.-211-6750A=
XM_005245393.5:c.89A=	XP_005245450.1:p.Asp30=
XM_011509832.2:c.-211-6750A=	XP_011508134.1:n.-211-6750A=
XM_017001955.2:c.89A=	XP_016857444.1:p.Asp30=
XM_017001956.1:c.-70A=	XP_016857445.1:n.-70A=
XM_017001957.1:c.-81A=	XP_016857446.1:n.-81A=
NM_021222.3:c.89A= MANE Select	NP_067045.1:p.Asp30=
NM_001303229.2:c.-255A=	NP_001290158.1:n.-255A=
NM_001303242.2:c.89A=	NP_001290171.1:p.Asp30=
NM_001303243.2:c.-171A=	NP_001290172.1:n.-171A=
NR_130130.2:n.224-7654A=
NR_130131.2:n.273A=
NR_130132.2:n.273A=
NR_130135.2:n.273A=