Canonical Allele Identifier: CA1207936917

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909622G= , CM000663.2:g.173909622G=	GRCh38
NC_000001.10:g.173878760G= , CM000663.1:g.173878760G=	GRCh37
NC_000001.9:g.172145383G=	NCBI36
NG_012462.1:g.12757C= , LRG_577:g.12757C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1083C= MANE Select	ENSP00000356671.3:p.Phe361=
ENST00000367698.3:c.1083C=	ENSP00000356671.3:p.Phe361=
ENST00000617423.4:c.560-2129C=	ENSP00000478688.1:n.560-2129C=
NM_000488.3:c.1083C= , LRG_577t1:c.1083C=	NP_000479.1:p.Phe361=
XM_005245198.2:c.939C=	XP_005245255.1:p.Phe313=
NM_001365052.1:c.939C=	NP_001351981.1:p.Phe313=
NM_000488.4:c.1083C= MANE Select	NP_000479.1:p.Phe361=
NM_001365052.2:c.939C=	NP_001351981.1:p.Phe313=
NM_001386302.1:c.1206C=	NP_001373231.1:p.Phe402=
NM_001386303.1:c.1164C=	NP_001373232.1:p.Phe388=
NM_001386304.1:c.1062C=	NP_001373233.1:p.Phe354=
NM_001386305.1:c.1026C=	NP_001373234.1:p.Phe342=
NM_001386306.1:c.867C=	NP_001373235.1:p.Phe289=