Canonical Allele Identifier: CA421942910

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1572088489
• MyVariant Identifiers: chr1:g.173878817T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909679T>C , CM000663.2:g.173909679T>C	GRCh38
NC_000001.10:g.173878817T>C , CM000663.1:g.173878817T>C	GRCh37
NC_000001.9:g.172145440T>C	NCBI36
NG_012462.1:g.12700A>G , LRG_577:g.12700A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1026A>G MANE Select	ENSP00000356671.3:p.Glu342=
ENST00000367698.3:c.1026A>G	ENSP00000356671.3:p.Glu342=
ENST00000617423.4:c.560-2186A>G	ENSP00000478688.1:n.560-2186A>G
NM_000488.3:c.1026A>G , LRG_577t1:c.1026A>G	NP_000479.1:p.Glu342=
XM_005245198.2:c.882A>G	XP_005245255.1:p.Glu294=
NM_001365052.1:c.882A>G	NP_001351981.1:p.Glu294=
NM_000488.4:c.1026A>G MANE Select	NP_000479.1:p.Glu342=
NM_001365052.2:c.882A>G	NP_001351981.1:p.Glu294=
NM_001386302.1:c.1149A>G	NP_001373231.1:p.Glu383=
NM_001386303.1:c.1107A>G	NP_001373232.1:p.Glu369=
NM_001386304.1:c.1005A>G	NP_001373233.1:p.Glu335=
NM_001386305.1:c.969A>G	NP_001373234.1:p.Glu323=
NM_001386306.1:c.810A>G	NP_001373235.1:p.Glu270=