Canonical Allele Identifier: CA2675565373
Gene: PURA HGNC NCBI

Linked Data

gnomAD v4: 5-140114168-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114168C>G , CM000667.2:g.140114168C>G GRCh38
NC_000005.9:g.139493753C>G , CM000667.1:g.139493753C>G GRCh37
NC_000005.8:g.139473937C>G NCBI36
NG_041813.1:g.5046C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.-14C>G MANE Select ENSP00000332706.3:n.-14C>G
ENST00000505703.2:c.-14C>G ENSP00000498560.1:n.-14C>G
ENST00000651386.1:c.-14C>G ENSP00000499133.1:n.-14C>G
ENST00000331327.4:c.-14C>G ENSP00000332706.3:n.-14C>G
ENST00000502351.1:n.410C>G
ENST00000505703.1:n.452C>G
NM_005859.4:c.-14C>G NP_005850.1:n.-14C>G
NM_005859.5:c.-14C>G MANE Select NP_005850.1:n.-14C>G
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