Canonical Allele Identifier: CA1729669533

Gene: SERPINE1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.101128442G= , CM000669.2:g.101128442G=	GRCh38
NC_000007.13:g.100771723G= , CM000669.1:g.100771723G=	GRCh37
NC_000007.12:g.100558443G=	NCBI36
NG_013213.1:g.6345G= , LRG_597:g.6345G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223095.5:c.49G= MANE Select	ENSP00000223095.4:p.Val17=
ENST00000223095.4:c.49G=	ENSP00000223095.4:p.Val17=
NM_000602.4:c.49G= , LRG_597t1:c.49G=	NP_000593.1:p.Val17=
NM_000602.5:c.49G= MANE Select	NP_000593.1:p.Val17=
NM_001386456.1:c.-32-172G=	NP_001373385.1:n.-32-172G=
NM_001386457.1:c.49G=	NP_001373386.1:p.Val17=
NM_001386458.1:c.49G=	NP_001373387.1:p.Val17=
NM_001386459.1:c.49G=	NP_001373388.1:p.Val17=
NM_001386460.1:c.49G=	NP_001373389.1:p.Val17=
NM_001386461.1:c.49G=	NP_001373390.1:p.Val17=
NM_001386462.1:c.-69-84G=	NP_001373391.1:n.-69-84G=
NM_001386463.1:c.43G=	NP_001373392.1:p.Val15=
NM_001386464.1:c.49G=	NP_001373393.1:p.Val17=
NM_001386465.1:c.49G=	NP_001373394.1:p.Val17=
NM_001386466.1:c.49G=	NP_001373395.1:p.Val17=