Canonical Allele Identifier: CA1729669463
Gene: SERPINE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.101128275C= , CM000669.2:g.101128275C= GRCh38
NC_000007.13:g.100771556C= , CM000669.1:g.100771556C= GRCh37
NC_000007.12:g.100558276C= NCBI36
NG_013213.1:g.6178C= , LRG_597:g.6178C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000223095.5:c.-1-118C= MANE Select ENSP00000223095.4:n.-1-118C=
ENST00000223095.4:c.-1-118C= ENSP00000223095.4:n.-1-118C=
NM_000602.4:c.-1-118C= , LRG_597t1:c.-1-118C= NP_000593.1:n.-1-118C=
NM_000602.5:c.-1-118C= MANE Select NP_000593.1:n.-1-118C=
NM_001386456.1:c.-32-339C= NP_001373385.1:n.-32-339C=
NM_001386457.1:c.-1-118C= NP_001373386.1:n.-1-118C=
NM_001386458.1:c.-1-118C= NP_001373387.1:n.-1-118C=
NM_001386459.1:c.-1-118C= NP_001373388.1:n.-1-118C=
NM_001386460.1:c.-1-118C= NP_001373389.1:n.-1-118C=
NM_001386461.1:c.-1-118C= NP_001373390.1:n.-1-118C=
NM_001386462.1:c.-69-251C= NP_001373391.1:n.-69-251C=
NM_001386463.1:c.1-125C= NP_001373392.1:n.1-125C=
NM_001386464.1:c.-1-118C= NP_001373393.1:n.-1-118C=
NM_001386465.1:c.-1-118C= NP_001373394.1:n.-1-118C=
NM_001386466.1:c.-1-118C= NP_001373395.1:n.-1-118C=