Canonical Allele Identifier: CA343772295

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173903956-A-C
• MyVariant Identifiers: chr1:g.173873094A>C (hg19) ; chr1:g.173903956A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903956A>C , CM000663.2:g.173903956A>C	GRCh38
NC_000001.10:g.173873094A>C , CM000663.1:g.173873094A>C	GRCh37
NC_000001.9:g.172139717A>C	NCBI36
NG_012462.1:g.18423T>G , LRG_577:g.18423T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1328T>G MANE Select	ENSP00000356671.3:p.Phe443Cys
ENST00000367698.3:c.1328T>G	ENSP00000356671.3:p.Phe443Cys
ENST00000617423.4:c.713T>G	ENSP00000478688.1:p.Phe238Cys
NM_000488.3:c.1328T>G , LRG_577t1:c.1328T>G	NP_000479.1:p.Phe443Cys
XM_005245198.2:c.1184T>G	XP_005245255.1:p.Phe395Cys
NM_001365052.1:c.1184T>G	NP_001351981.1:p.Phe395Cys
NM_000488.4:c.1328T>G MANE Select	NP_000479.1:p.Phe443Cys
NM_001365052.2:c.1184T>G	NP_001351981.1:p.Phe395Cys
NM_001386302.1:c.1451T>G	NP_001373231.1:p.Phe484Cys
NM_001386303.1:c.1409T>G	NP_001373232.1:p.Phe470Cys
NM_001386304.1:c.1307T>G	NP_001373233.1:p.Phe436Cys
NM_001386305.1:c.1271T>G	NP_001373234.1:p.Phe424Cys
NM_001386306.1:c.1112T>G	NP_001373235.1:p.Phe371Cys