Canonical Allele Identifier: CA13062452
Gene: PLAA HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12003612

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.26940725C>T , CM000671.2:g.26940725C>T GRCh38
NC_000009.11:g.26940723C>T , CM000671.1:g.26940723C>T GRCh37
NC_000009.10:g.26930723C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001031689.2:c.150-5519G>A VV NP_001026859.1:p.=
XM_011518071.1:c.150-5519G>A XP_011516373.1:p.=
XM_011518072.1:c.150-5519G>A XP_011516374.1:p.=
NM_001321546.1:c.150-5519G>A VV NP_001308475.1:p.=
XM_011518072.3:c.150-5519G>A XP_011516374.1:p.=
XM_017015319.2:c.150-5519G>A XP_016870808.1:p.=
XR_001746420.2:n.372-5519G>A
NM_001031689.3:c.150-5519G>A VV MANE Preferred NP_001026859.1:p.=
ENST00000397292.7:c.150-5519G>A ENSP00000380460.3:p.=
ENST00000520884.5:c.150-5519G>A ENSP00000429372.1:p.=
ENST00000523212.1:n.88-5528G>A