Canonical Allele Identifier: CA456771407
Gene: SERPINE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.100771719C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.101128438C>A , CM000669.2:g.101128438C>A GRCh38
NC_000007.13:g.100771719C>A , CM000669.1:g.100771719C>A GRCh37
NC_000007.12:g.100558439C>A NCBI36
NG_013213.1:g.6341C>A , LRG_597:g.6341C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000223095.5:c.45C>A MANE Select ENSP00000223095.4:p.Ala15=
ENST00000223095.4:c.45C>A ENSP00000223095.4:p.Ala15=
NM_000602.4:c.45C>A , LRG_597t1:c.45C>A NP_000593.1:p.Ala15=
NM_000602.5:c.45C>A MANE Select NP_000593.1:p.Ala15=
NM_001386456.1:c.-32-176C>A NP_001373385.1:n.-32-176C>A
NM_001386457.1:c.45C>A NP_001373386.1:p.Ala15=
NM_001386458.1:c.45C>A NP_001373387.1:p.Ala15=
NM_001386459.1:c.45C>A NP_001373388.1:p.Ala15=
NM_001386460.1:c.45C>A NP_001373389.1:p.Ala15=
NM_001386461.1:c.45C>A NP_001373390.1:p.Ala15=
NM_001386462.1:c.-69-88C>A NP_001373391.1:n.-69-88C>A
NM_001386463.1:c.39C>A NP_001373392.1:p.Ala13=
NM_001386464.1:c.45C>A NP_001373393.1:p.Ala15=
NM_001386465.1:c.45C>A NP_001373394.1:p.Ala15=
NM_001386466.1:c.45C>A NP_001373395.1:p.Ala15=