Canonical Allele Identifier: CA1207936955

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909702C= , CM000663.2:g.173909702C=	GRCh38
NC_000001.10:g.173878840C= , CM000663.1:g.173878840C=	GRCh37
NC_000001.9:g.172145463C=	NCBI36
NG_012462.1:g.12677G= , LRG_577:g.12677G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1003G= MANE Select	ENSP00000356671.3:p.Val335=
ENST00000367698.3:c.1003G=	ENSP00000356671.3:p.Val335=
ENST00000617423.4:c.559+2162G=	ENSP00000478688.1:n.559+2162G=
NM_000488.3:c.1003G= , LRG_577t1:c.1003G=	NP_000479.1:p.Val335=
XM_005245198.2:c.859G=	XP_005245255.1:p.Val287=
NM_001365052.1:c.859G=	NP_001351981.1:p.Val287=
NM_000488.4:c.1003G= MANE Select	NP_000479.1:p.Val335=
NM_001365052.2:c.859G=	NP_001351981.1:p.Val287=
NM_001386302.1:c.1126G=	NP_001373231.1:p.Val376=
NM_001386303.1:c.1084G=	NP_001373232.1:p.Val362=
NM_001386304.1:c.982G=	NP_001373233.1:p.Val328=
NM_001386305.1:c.946G=	NP_001373234.1:p.Val316=
NM_001386306.1:c.787G=	NP_001373235.1:p.Val263=