Canonical Allele Identifier: CA1148335118

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173912001T= , CM000663.2:g.173912001T=	GRCh38
NC_000001.10:g.173881139T= , CM000663.1:g.173881139T=	GRCh37
NC_000001.9:g.172147762T=	NCBI36
NG_012462.1:g.10378A= , LRG_577:g.10378A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.422A= MANE Select	ENSP00000356671.3:p.Asp141=
ENST00000367698.3:c.422A=	ENSP00000356671.3:p.Asp141=
ENST00000487183.1:n.127A=
ENST00000494024.1:n.648A=
ENST00000617423.4:c.422A=	ENSP00000478688.1:p.Asp141=
NM_000488.3:c.422A= , LRG_577t1:c.422A=	NP_000479.1:p.Asp141=
XM_005245198.2:c.278A=	XP_005245255.1:p.Asp93=
NM_001365052.1:c.278A=	NP_001351981.1:p.Asp93=
NM_000488.4:c.422A= MANE Select	NP_000479.1:p.Asp141=
NM_001365052.2:c.278A=	NP_001351981.1:p.Asp93=
NM_001386302.1:c.422A=	NP_001373231.1:p.Asp141=
NM_001386303.1:c.503A=	NP_001373232.1:p.Asp168=
NM_001386304.1:c.422A=	NP_001373233.1:p.Asp141=
NM_001386305.1:c.422A=	NP_001373234.1:p.Asp141=
NM_001386306.1:c.409-1110A=	NP_001373235.1:n.409-1110A=