Canonical Allele Identifier: CA1207934375

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903964G= , CM000663.2:g.173903964G=	GRCh38
NC_000001.10:g.173873102G= , CM000663.1:g.173873102G=	GRCh37
NC_000001.9:g.172139725G=	NCBI36
NG_012462.1:g.18415C= , LRG_577:g.18415C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1320C= MANE Select	ENSP00000356671.3:p.Phe440=
ENST00000367698.3:c.1320C=	ENSP00000356671.3:p.Phe440=
ENST00000617423.4:c.705C=	ENSP00000478688.1:p.Phe235=
NM_000488.3:c.1320C= , LRG_577t1:c.1320C=	NP_000479.1:p.Phe440=
XM_005245198.2:c.1176C=	XP_005245255.1:p.Phe392=
NM_001365052.1:c.1176C=	NP_001351981.1:p.Phe392=
NM_000488.4:c.1320C= MANE Select	NP_000479.1:p.Phe440=
NM_001365052.2:c.1176C=	NP_001351981.1:p.Phe392=
NM_001386302.1:c.1443C=	NP_001373231.1:p.Phe481=
NM_001386303.1:c.1401C=	NP_001373232.1:p.Phe467=
NM_001386304.1:c.1299C=	NP_001373233.1:p.Phe433=
NM_001386305.1:c.1263C=	NP_001373234.1:p.Phe421=
NM_001386306.1:c.1104C=	NP_001373235.1:p.Phe368=