Canonical Allele Identifier: CA1729674422
Gene: SERPINE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.101137803T= , CM000669.2:g.101137803T= GRCh38
NC_000007.13:g.100781084T= , CM000669.1:g.100781084T= GRCh37
NC_000007.12:g.100567804T= NCBI36
NG_013213.1:g.15706T= , LRG_597:g.15706T=

Transcript Alleles

HGVS Amino-acid Change
NM_000602.5:c.*361T= MANE Select NP_000593.1:n.*361T=
ENST00000223095.5:c.*361T= MANE Select ENSP00000223095.4:n.*361T=
NM_000602.4:c.*361T= , LRG_597t1:c.*361T= NP_000593.1:n.*361T=
NM_001386456.1:c.*361T= NP_001373385.1:n.*361T=
NM_001386457.1:c.*372T= NP_001373386.1:n.*372T=
NM_001386458.1:c.*361T= NP_001373387.1:n.*361T=
NM_001386459.1:c.1195-205T= NP_001373388.1:n.1195-205T=
NM_001386460.1:c.1185T= NP_001373389.1:p.Asp395=
NM_001386461.1:c.1088-20T= NP_001373390.1:n.1088-20T=
NM_001386462.1:c.*361T= NP_001373391.1:n.*361T=
NM_001386463.1:c.*361T= NP_001373392.1:n.*361T=
NM_001386464.1:c.*452T= NP_001373393.1:n.*452T=
NM_001386465.1:c.*361T= NP_001373394.1:n.*361T=
NM_001386466.1:c.*361T= NP_001373395.1:n.*361T=
ENST00000223095.4:c.*361T= ENSP00000223095.4:n.*361T=