Canonical Allele Identifier: CA1207934403

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904078T= , CM000663.2:g.173904078T=	GRCh38
NC_000001.10:g.173873216T= , CM000663.1:g.173873216T=	GRCh37
NC_000001.9:g.172139839T=	NCBI36
NG_012462.1:g.18301A= , LRG_577:g.18301A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1219-13A= MANE Select	ENSP00000356671.3:n.1219-13A=
ENST00000367698.3:c.1219-13A=	ENSP00000356671.3:n.1219-13A=
ENST00000617423.4:c.604-13A=	ENSP00000478688.1:n.604-13A=
NM_000488.3:c.1219-13A= , LRG_577t1:c.1219-13A=	NP_000479.1:n.1219-13A=
XM_005245198.2:c.1075-13A=	XP_005245255.1:n.1075-13A=
NM_001365052.1:c.1075-13A=	NP_001351981.1:n.1075-13A=
NM_000488.4:c.1219-13A= MANE Select	NP_000479.1:n.1219-13A=
NM_001365052.2:c.1075-13A=	NP_001351981.1:n.1075-13A=
NM_001386302.1:c.1342-13A=	NP_001373231.1:n.1342-13A=
NM_001386303.1:c.1300-13A=	NP_001373232.1:n.1300-13A=
NM_001386304.1:c.1198-13A=	NP_001373233.1:n.1198-13A=
NM_001386305.1:c.1162-13A=	NP_001373234.1:n.1162-13A=
NM_001386306.1:c.1003-13A=	NP_001373235.1:n.1003-13A=