Canonical Allele Identifier: CA2675565291

Gene: PURA

Linked Data

• gnomAD v4: 5-140114138-G-GGCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140114138_140114139insGCCC , CM000667.2:g.140114138_140114139insGCCC	GRCh38
NC_000005.9:g.139493723_139493724insGCCC , CM000667.1:g.139493723_139493724insGCCC	GRCh37
NC_000005.8:g.139473907_139473908insGCCC	NCBI36
NG_041813.1:g.5016_5017insGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331327.5:c.-44_-43insGCCC MANE Select	ENSP00000332706.3:n.-44_-43insGCCC
ENST00000505703.2:c.-44_-43insGCCC	ENSP00000498560.1:n.-44_-43insGCCC
ENST00000651386.1:c.-44_-43insGCCC	ENSP00000499133.1:n.-44_-43insGCCC
ENST00000331327.4:c.-44_-43insGCCC	ENSP00000332706.3:n.-44_-43insGCCC
ENST00000502351.1:n.380_381insGCCC
ENST00000505703.1:n.422_423insGCCC
NM_005859.4:c.-44_-43insGCCC	NP_005850.1:n.-44_-43insGCCC
NM_005859.5:c.-44_-43insGCCC MANE Select	NP_005850.1:n.-44_-43insGCCC