Canonical Allele Identifier: CA446831218
Gene: PURA HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.139494162G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114577G>C , CM000667.2:g.140114577G>C GRCh38
NC_000005.9:g.139494162G>C , CM000667.1:g.139494162G>C GRCh37
NC_000005.8:g.139474346G>C NCBI36
NG_041813.1:g.5455G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000331327.5:c.396G>C MANE Select ENSP00000332706.3:p.Leu132=
ENST00000651386.1:c.396G>C ENSP00000499133.1:p.Leu132=
ENST00000331327.4:c.396G>C ENSP00000332706.3:p.Leu132=
NM_005859.4:c.396G>C NP_005850.1:p.Leu132=
NM_005859.5:c.396G>C MANE Select NP_005850.1:p.Leu132=
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