Canonical Allele Identifier: CA343774734

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173879040T>C (hg19) ; chr1:g.173909902T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909902T>C , CM000663.2:g.173909902T>C	GRCh38
NC_000001.10:g.173879040T>C , CM000663.1:g.173879040T>C	GRCh37
NC_000001.9:g.172145663T>C	NCBI36
NG_012462.1:g.12477A>G , LRG_577:g.12477A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.803A>G MANE Select	ENSP00000356671.3:p.Lys268Arg
ENST00000367698.3:c.803A>G	ENSP00000356671.3:p.Lys268Arg
ENST00000487183.1:n.454A>G
ENST00000617423.4:c.559+1962A>G	ENSP00000478688.1:n.559+1962A>G
NM_000488.3:c.803A>G , LRG_577t1:c.803A>G	NP_000479.1:p.Lys268Arg
XM_005245198.2:c.659A>G	XP_005245255.1:p.Lys220Arg
NM_001365052.1:c.659A>G	NP_001351981.1:p.Lys220Arg
NM_000488.4:c.803A>G MANE Select	NP_000479.1:p.Lys268Arg
NM_001365052.2:c.659A>G	NP_001351981.1:p.Lys220Arg
NM_001386302.1:c.926A>G	NP_001373231.1:p.Lys309Arg
NM_001386303.1:c.884A>G	NP_001373232.1:p.Lys295Arg
NM_001386304.1:c.782A>G	NP_001373233.1:p.Lys261Arg
NM_001386305.1:c.763-17A>G	NP_001373234.1:n.763-17A>G
NM_001386306.1:c.587A>G	NP_001373235.1:p.Lys196Arg