Canonical Allele Identifier: CA361490818
Gene: PURA HGNC NCBI

Linked Data

ClinVar Variation Id: 2070656
ClinVar RCV Id: RCV002971318

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140114642A>G , CM000667.2:g.140114642A>G GRCh38
NC_000005.9:g.139494227A>G , CM000667.1:g.139494227A>G GRCh37
NC_000005.8:g.139474411A>G NCBI36
NG_041813.1:g.5520A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331327.5:c.461A>G MANE Select ENSP00000332706.3:p.Lys154Arg
ENST00000651386.1:c.461A>G ENSP00000499133.1:p.Lys154Arg
ENST00000331327.4:c.461A>G ENSP00000332706.3:p.Lys154Arg
NM_005859.4:c.461A>G NP_005850.1:p.Lys154Arg
NM_005859.5:c.461A>G MANE Select NP_005850.1:p.Lys154Arg