Canonical Allele Identifier: CA1207934371

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903954T= , CM000663.2:g.173903954T=	GRCh38
NC_000001.10:g.173873092T= , CM000663.1:g.173873092T=	GRCh37
NC_000001.9:g.172139715T=	NCBI36
NG_012462.1:g.18425A= , LRG_577:g.18425A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1330A= MANE Select	ENSP00000356671.3:p.Ile444=
ENST00000367698.3:c.1330A=	ENSP00000356671.3:p.Ile444=
ENST00000617423.4:c.715A=	ENSP00000478688.1:p.Ile239=
NM_000488.3:c.1330A= , LRG_577t1:c.1330A=	NP_000479.1:p.Ile444=
XM_005245198.2:c.1186A=	XP_005245255.1:p.Ile396=
NM_001365052.1:c.1186A=	NP_001351981.1:p.Ile396=
NM_000488.4:c.1330A= MANE Select	NP_000479.1:p.Ile444=
NM_001365052.2:c.1186A=	NP_001351981.1:p.Ile396=
NM_001386302.1:c.1453A=	NP_001373231.1:p.Ile485=
NM_001386303.1:c.1411A=	NP_001373232.1:p.Ile471=
NM_001386304.1:c.1309A=	NP_001373233.1:p.Ile437=
NM_001386305.1:c.1273A=	NP_001373234.1:p.Ile425=
NM_001386306.1:c.1114A=	NP_001373235.1:p.Ile372=