Canonical Allele Identifier: CA446830960
Gene: PURA HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.139494288C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114703C>T , CM000667.2:g.140114703C>T GRCh38
NC_000005.9:g.139494288C>T , CM000667.1:g.139494288C>T GRCh37
NC_000005.8:g.139474472C>T NCBI36
NG_041813.1:g.5581C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000331327.5:c.522C>T MANE Select ENSP00000332706.3:p.Val174=
ENST00000651386.1:c.522C>T ENSP00000499133.1:p.Val174=
ENST00000331327.4:c.522C>T ENSP00000332706.3:p.Val174=
NM_005859.4:c.522C>T NP_005850.1:p.Val174=
NM_005859.5:c.522C>T MANE Select NP_005850.1:p.Val174=