Canonical Allele Identifier: CA163332430

Gene: SERPINE1

Linked Data

• dbSNP Id: rs775667537
• MyVariant Identifiers: chr7:g.100774766C>A (hg19) ; chr7:g.101131485C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.101131485C>A , CM000669.2:g.101131485C>A	GRCh38
NC_000007.13:g.100774766C>A , CM000669.1:g.100774766C>A	GRCh37
NC_000007.12:g.100561486C>A	NCBI36
NG_013213.1:g.9388C>A , LRG_597:g.9388C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000223095.5:c.506-390C>A MANE Select	ENSP00000223095.4:n.506-390C>A
ENST00000223095.4:c.506-390C>A	ENSP00000223095.4:n.506-390C>A
NM_000602.4:c.506-390C>A , LRG_597t1:c.506-390C>A	NP_000593.1:n.506-390C>A
NM_000602.5:c.506-390C>A MANE Select	NP_000593.1:n.506-390C>A
NM_001386456.1:c.254-390C>A	NP_001373385.1:n.254-390C>A
NM_001386457.1:c.506-390C>A	NP_001373386.1:n.506-390C>A
NM_001386458.1:c.506-390C>A	NP_001373387.1:n.506-390C>A
NM_001386459.1:c.506-390C>A	NP_001373388.1:n.506-390C>A
NM_001386460.1:c.506-390C>A	NP_001373389.1:n.506-390C>A
NM_001386461.1:c.506-390C>A	NP_001373390.1:n.506-390C>A
NM_001386462.1:c.305-390C>A	NP_001373391.1:n.305-390C>A
NM_001386463.1:c.500-390C>A	NP_001373392.1:n.500-390C>A
NM_001386464.1:c.506-390C>A	NP_001373393.1:n.506-390C>A
NM_001386465.1:c.506-390C>A	NP_001373394.1:n.506-390C>A
NM_001386466.1:c.530-390C>A	NP_001373395.1:n.530-390C>A