Canonical Allele Identifier: CA1586594082

Gene: PURA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140114484T= , CM000667.2:g.140114484T=	GRCh38
NC_000005.9:g.139494069T= , CM000667.1:g.139494069T=	GRCh37
NC_000005.8:g.139474253T=	NCBI36
NG_041813.1:g.5362T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000331327.5:c.303T= MANE Select	ENSP00000332706.3:p.Thr101=
ENST00000505703.2:c.303T=	ENSP00000498560.1:p.Thr101=
ENST00000651386.1:c.303T=	ENSP00000499133.1:p.Thr101=
ENST00000331327.4:c.303T=	ENSP00000332706.3:p.Thr101=
NM_005859.4:c.303T=	NP_005850.1:p.Thr101=
NM_005859.5:c.303T= MANE Select	NP_005850.1:p.Thr101=