Canonical Allele Identifier: CA15500288

Gene: SERPINE1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.101132405G>T , CM000669.2:g.101132405G>T	GRCh38
NC_000007.13:g.100775686G>T , CM000669.1:g.100775686G>T	GRCh37
NC_000007.12:g.100562406G>T	NCBI36
NG_013213.1:g.10308G>T , LRG_597:g.10308G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223095.5:c.700+336G>T MANE Select	ENSP00000223095.4:n.700+336G>T
ENST00000223095.4:c.700+336G>T	ENSP00000223095.4:n.700+336G>T
NM_000602.4:c.700+336G>T , LRG_597t1:c.700+336G>T	NP_000593.1:n.700+336G>T
NM_000602.5:c.700+336G>T MANE Select	NP_000593.1:n.700+336G>T
NM_001386456.1:c.448+336G>T	NP_001373385.1:n.448+336G>T
NM_001386457.1:c.700+336G>T	NP_001373386.1:n.700+336G>T
NM_001386458.1:c.700+336G>T	NP_001373387.1:n.700+336G>T
NM_001386459.1:c.700+336G>T	NP_001373388.1:n.700+336G>T
NM_001386460.1:c.700+336G>T	NP_001373389.1:n.700+336G>T
NM_001386461.1:c.700+336G>T	NP_001373390.1:n.700+336G>T
NM_001386462.1:c.499+336G>T	NP_001373391.1:n.499+336G>T
NM_001386463.1:c.694+336G>T	NP_001373392.1:n.694+336G>T
NM_001386464.1:c.700+336G>T	NP_001373393.1:n.700+336G>T
NM_001386465.1:c.700+336G>T	NP_001373394.1:n.700+336G>T
NM_001386466.1:c.724+336G>T	NP_001373395.1:n.724+336G>T