Canonical Allele Identifier: CA361490799

Gene: PURA

Linked Data

• MyVariant Identifiers: chr5:g.139494219G>C (hg19) ; chr5:g.140114634G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140114634G>C , CM000667.2:g.140114634G>C	GRCh38
NC_000005.9:g.139494219G>C , CM000667.1:g.139494219G>C	GRCh37
NC_000005.8:g.139474403G>C	NCBI36
NG_041813.1:g.5512G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331327.5:c.453G>C MANE Select	ENSP00000332706.3:p.Glu151Asp
ENST00000651386.1:c.453G>C	ENSP00000499133.1:p.Glu151Asp
ENST00000331327.4:c.453G>C	ENSP00000332706.3:p.Glu151Asp
NM_005859.4:c.453G>C	NP_005850.1:p.Glu151Asp
NM_005859.5:c.453G>C MANE Select	NP_005850.1:p.Glu151Asp