Canonical Allele Identifier: CA1729671049

Gene: SERPINE1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.101131387C= , CM000669.2:g.101131387C=	GRCh38
NC_000007.13:g.100774668C= , CM000669.1:g.100774668C=	GRCh37
NC_000007.12:g.100561388C=	NCBI36
NG_013213.1:g.9290C= , LRG_597:g.9290C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223095.5:c.506-488C= MANE Select	ENSP00000223095.4:n.506-488C=
ENST00000223095.4:c.506-488C=	ENSP00000223095.4:n.506-488C=
NM_000602.4:c.506-488C= , LRG_597t1:c.506-488C=	NP_000593.1:n.506-488C=
NM_000602.5:c.506-488C= MANE Select	NP_000593.1:n.506-488C=
NM_001386456.1:c.254-488C=	NP_001373385.1:n.254-488C=
NM_001386457.1:c.506-488C=	NP_001373386.1:n.506-488C=
NM_001386458.1:c.506-488C=	NP_001373387.1:n.506-488C=
NM_001386459.1:c.506-488C=	NP_001373388.1:n.506-488C=
NM_001386460.1:c.506-488C=	NP_001373389.1:n.506-488C=
NM_001386461.1:c.506-488C=	NP_001373390.1:n.506-488C=
NM_001386462.1:c.305-488C=	NP_001373391.1:n.305-488C=
NM_001386463.1:c.500-488C=	NP_001373392.1:n.500-488C=
NM_001386464.1:c.506-488C=	NP_001373393.1:n.506-488C=
NM_001386465.1:c.506-488C=	NP_001373394.1:n.506-488C=
NM_001386466.1:c.530-488C=	NP_001373395.1:n.530-488C=