Canonical Allele Identifier: CA163332426

Gene: SERPINE1

Linked Data

• dbSNP Id: rs941764673
• MyVariant Identifiers: chr7:g.100774751T>C (hg19) ; chr7:g.101131470T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.101131470T>C , CM000669.2:g.101131470T>C	GRCh38
NC_000007.13:g.100774751T>C , CM000669.1:g.100774751T>C	GRCh37
NC_000007.12:g.100561471T>C	NCBI36
NG_013213.1:g.9373T>C , LRG_597:g.9373T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000223095.5:c.506-405T>C MANE Select	ENSP00000223095.4:n.506-405T>C
ENST00000223095.4:c.506-405T>C	ENSP00000223095.4:n.506-405T>C
NM_000602.4:c.506-405T>C , LRG_597t1:c.506-405T>C	NP_000593.1:n.506-405T>C
NM_000602.5:c.506-405T>C MANE Select	NP_000593.1:n.506-405T>C
NM_001386456.1:c.254-405T>C	NP_001373385.1:n.254-405T>C
NM_001386457.1:c.506-405T>C	NP_001373386.1:n.506-405T>C
NM_001386458.1:c.506-405T>C	NP_001373387.1:n.506-405T>C
NM_001386459.1:c.506-405T>C	NP_001373388.1:n.506-405T>C
NM_001386460.1:c.506-405T>C	NP_001373389.1:n.506-405T>C
NM_001386461.1:c.506-405T>C	NP_001373390.1:n.506-405T>C
NM_001386462.1:c.305-405T>C	NP_001373391.1:n.305-405T>C
NM_001386463.1:c.500-405T>C	NP_001373392.1:n.500-405T>C
NM_001386464.1:c.506-405T>C	NP_001373393.1:n.506-405T>C
NM_001386465.1:c.506-405T>C	NP_001373394.1:n.506-405T>C
NM_001386466.1:c.530-405T>C	NP_001373395.1:n.530-405T>C