Canonical Allele Identifier: CA1729673464

Gene: SERPINE1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.101135963C= , CM000669.2:g.101135963C=	GRCh38
NC_000007.13:g.100779244C= , CM000669.1:g.100779244C=	GRCh37
NC_000007.12:g.100565964C=	NCBI36
NG_013213.1:g.13866C= , LRG_597:g.13866C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223095.5:c.1087+162C= MANE Select	ENSP00000223095.4:n.1087+162C=
ENST00000223095.4:c.1087+162C=	ENSP00000223095.4:n.1087+162C=
NM_000602.4:c.1087+162C= , LRG_597t1:c.1087+162C=	NP_000593.1:n.1087+162C=
NM_000602.5:c.1087+162C= MANE Select	NP_000593.1:n.1087+162C=
NM_001386456.1:c.835+162C=	NP_001373385.1:n.835+162C=
NM_001386457.1:c.1000+369C=	NP_001373386.1:n.1000+369C=
NM_001386458.1:c.1087+162C=	NP_001373387.1:n.1087+162C=
NM_001386459.1:c.1087+162C=	NP_001373388.1:n.1087+162C=
NM_001386460.1:c.1087+162C=	NP_001373389.1:n.1087+162C=
NM_001386461.1:c.1087+162C=	NP_001373390.1:n.1087+162C=
NM_001386462.1:c.886+162C=	NP_001373391.1:n.886+162C=
NM_001386463.1:c.1081+162C=	NP_001373392.1:n.1081+162C=
NM_001386464.1:c.1087+162C=	NP_001373393.1:n.1087+162C=
NM_001386465.1:c.1102+147C=	NP_001373394.1:n.1102+147C=
NM_001386466.1:c.1111+162C=	NP_001373395.1:n.1111+162C=