Canonical Allele Identifier: CA456771575

Gene: SERPINE1

Linked Data

• MyVariant Identifiers: chr7:g.100771821C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.101128540C>A , CM000669.2:g.101128540C>A	GRCh38
NC_000007.13:g.100771821C>A , CM000669.1:g.100771821C>A	GRCh37
NC_000007.12:g.100558541C>A	NCBI36
NG_013213.1:g.6443C>A , LRG_597:g.6443C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223095.5:c.147C>A MANE Select	ENSP00000223095.4:p.Ala49=
ENST00000223095.4:c.147C>A	ENSP00000223095.4:p.Ala49=
NM_000602.4:c.147C>A , LRG_597t1:c.147C>A	NP_000593.1:p.Ala49=
NM_000602.5:c.147C>A MANE Select	NP_000593.1:p.Ala49=
NM_001386456.1:c.-32-74C>A	NP_001373385.1:n.-32-74C>A
NM_001386457.1:c.147C>A	NP_001373386.1:p.Ala49=
NM_001386458.1:c.147C>A	NP_001373387.1:p.Ala49=
NM_001386459.1:c.147C>A	NP_001373388.1:p.Ala49=
NM_001386460.1:c.147C>A	NP_001373389.1:p.Ala49=
NM_001386461.1:c.147C>A	NP_001373390.1:p.Ala49=
NM_001386462.1:c.-55C>A	NP_001373391.1:n.-55C>A
NM_001386463.1:c.141C>A	NP_001373392.1:p.Ala47=
NM_001386464.1:c.147C>A	NP_001373393.1:p.Ala49=
NM_001386465.1:c.147C>A	NP_001373394.1:p.Ala49=
NM_001386466.1:c.147C>A	NP_001373395.1:p.Ala49=