Canonical Allele Identifier: CA446831036
Gene: PURA HGNC NCBI

Linked Data

ClinVar Variation Id: 2655736
ClinVar RCV Id: RCV003436459
MyVariant Identifiers: chr5:g.139494072C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114487C>G , CM000667.2:g.140114487C>G GRCh38
NC_000005.9:g.139494072C>G , CM000667.1:g.139494072C>G GRCh37
NC_000005.8:g.139474256C>G NCBI36
NG_041813.1:g.5365C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000331327.5:c.306C>G MANE Select ENSP00000332706.3:p.Leu102=
ENST00000505703.2:c.306C>G ENSP00000498560.1:p.Leu102=
ENST00000651386.1:c.306C>G ENSP00000499133.1:p.Leu102=
ENST00000331327.4:c.306C>G ENSP00000332706.3:p.Leu102=
NM_005859.4:c.306C>G NP_005850.1:p.Leu102=
NM_005859.5:c.306C>G MANE Select NP_005850.1:p.Leu102=
Search 100 bp 5'
Search 100 bp 3'