Canonical Allele Identifier: CA421942903

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1572088474
• MyVariant Identifiers: chr1:g.173878811C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909673C>T , CM000663.2:g.173909673C>T	GRCh38
NC_000001.10:g.173878811C>T , CM000663.1:g.173878811C>T	GRCh37
NC_000001.9:g.172145434C>T	NCBI36
NG_012462.1:g.12706G>A , LRG_577:g.12706G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1032G>A MANE Select	ENSP00000356671.3:p.Glu344=
ENST00000367698.3:c.1032G>A	ENSP00000356671.3:p.Glu344=
ENST00000617423.4:c.560-2180G>A	ENSP00000478688.1:n.560-2180G>A
NM_000488.3:c.1032G>A , LRG_577t1:c.1032G>A	NP_000479.1:p.Glu344=
XM_005245198.2:c.888G>A	XP_005245255.1:p.Glu296=
NM_001365052.1:c.888G>A	NP_001351981.1:p.Glu296=
NM_000488.4:c.1032G>A MANE Select	NP_000479.1:p.Glu344=
NM_001365052.2:c.888G>A	NP_001351981.1:p.Glu296=
NM_001386302.1:c.1155G>A	NP_001373231.1:p.Glu385=
NM_001386303.1:c.1113G>A	NP_001373232.1:p.Glu371=
NM_001386304.1:c.1011G>A	NP_001373233.1:p.Glu337=
NM_001386305.1:c.975G>A	NP_001373234.1:p.Glu325=
NM_001386306.1:c.816G>A	NP_001373235.1:p.Glu272=