Canonical Allele Identifier: CA420726914

Gene: PRUNE1

Linked Data

• MyVariant Identifiers: chr1:g.150990365T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151017889T>C , CM000663.2:g.151017889T>C	GRCh38
NC_000001.10:g.150990365T>C , CM000663.1:g.150990365T>C	GRCh37
NC_000001.9:g.149256989T>C	NCBI36
NG_052875.1:g.14499T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271620.8:c.117T>C MANE Select	ENSP00000271620.3:p.Ala39=
ENST00000650332.1:c.117T>C	ENSP00000497847.1:p.Ala39=
ENST00000271620.7:c.117T>C	ENSP00000271620.3:p.Ala39=
ENST00000368935.1:c.-33T>C	ENSP00000357931.1:n.-33T>C
ENST00000368936.5:c.-227T>C	ENSP00000357932.1:n.-227T>C
ENST00000368937.5:c.-26-7626T>C	ENSP00000357933.1:n.-26-7626T>C
ENST00000431193.5:c.-42T>C	ENSP00000392632.1:n.-42T>C
ENST00000450884.5:c.-211-6722T>C	ENSP00000387696.1:n.-211-6722T>C
ENST00000462440.5:n.300T>C
ENST00000467771.5:n.330T>C
ENST00000475722.5:n.283T>C
NM_001303229.1:c.-227T>C	NP_001290158.1:n.-227T>C
NM_001303242.1:c.117T>C	NP_001290171.1:p.Ala39=
NM_001303243.1:c.-143T>C	NP_001290172.1:n.-143T>C
NM_021222.2:c.117T>C	NP_067045.1:p.Ala39=
NR_130130.1:n.282-7626T>C
NR_130131.1:n.359T>C
NR_130132.1:n.359T>C
NR_130135.1:n.359T>C
XM_005245393.3:c.117T>C	XP_005245450.1:p.Ala39=
XM_005245397.3:c.-42T>C	XP_005245454.1:n.-42T>C
XM_011509830.1:c.117T>C	XP_011508132.1:p.Ala39=
XM_011509831.1:c.-53T>C	XP_011508133.1:n.-53T>C
XM_011509832.1:c.-211-6722T>C	XP_011508134.1:n.-211-6722T>C
XM_005245393.5:c.117T>C	XP_005245450.1:p.Ala39=
XM_011509832.2:c.-211-6722T>C	XP_011508134.1:n.-211-6722T>C
XM_017001955.2:c.117T>C	XP_016857444.1:p.Ala39=
XM_017001956.1:c.-42T>C	XP_016857445.1:n.-42T>C
XM_017001957.1:c.-53T>C	XP_016857446.1:n.-53T>C
NM_021222.3:c.117T>C MANE Select	NP_067045.1:p.Ala39=
NM_001303229.2:c.-227T>C	NP_001290158.1:n.-227T>C
NM_001303242.2:c.117T>C	NP_001290171.1:p.Ala39=
NM_001303243.2:c.-143T>C	NP_001290172.1:n.-143T>C
NR_130130.2:n.224-7626T>C
NR_130131.2:n.301T>C
NR_130132.2:n.301T>C
NR_130135.2:n.301T>C