Canonical Allele Identifier: CA1729674580

Gene: SERPINE1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.101138164T= , CM000669.2:g.101138164T=	GRCh38
NC_000007.13:g.100781445T= , CM000669.1:g.100781445T=	GRCh37
NC_000007.12:g.100568165T=	NCBI36
NG_013213.1:g.16067T= , LRG_597:g.16067T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000602.5:c.*722T= MANE Select	NP_000593.1:n.*722T=
ENST00000223095.5:c.*722T= MANE Select	ENSP00000223095.4:n.*722T=
NM_000602.4:c.*722T= , LRG_597t1:c.*722T=	NP_000593.1:n.*722T=
NM_001386456.1:c.*722T=	NP_001373385.1:n.*722T=
NM_001386457.1:c.*733T=	NP_001373386.1:n.*733T=
NM_001386458.1:c.*722T=	NP_001373387.1:n.*722T=
NM_001386459.1:c.*67T=	NP_001373388.1:n.*67T=
NM_001386460.1:c.*67T=	NP_001373389.1:n.*67T=
NM_001386461.1:c.*67T=	NP_001373390.1:n.*67T=
NM_001386462.1:c.*722T=	NP_001373391.1:n.*722T=
NM_001386463.1:c.*722T=	NP_001373392.1:n.*722T=
NM_001386464.1:c.*813T=	NP_001373393.1:n.*813T=
NM_001386465.1:c.*722T=	NP_001373394.1:n.*722T=
NM_001386466.1:c.*722T=	NP_001373395.1:n.*722T=
ENST00000223095.4:c.*722T=	ENSP00000223095.4:n.*722T=