Canonical Allele Identifier: CA1139773039

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903934G= , CM000663.2:g.173903934G=	GRCh38
NC_000001.10:g.173873072G= , CM000663.1:g.173873072G=	GRCh37
NC_000001.9:g.172139695G=	NCBI36
NG_012462.1:g.18445C= , LRG_577:g.18445C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1350C= MANE Select	ENSP00000356671.3:p.Asn450=
ENST00000367698.3:c.1350C=	ENSP00000356671.3:p.Asn450=
ENST00000617423.4:c.735C=	ENSP00000478688.1:p.Asn245=
NM_000488.3:c.1350C= , LRG_577t1:c.1350C=	NP_000479.1:p.Asn450=
XM_005245198.2:c.1206C=	XP_005245255.1:p.Asn402=
NM_001365052.1:c.1206C=	NP_001351981.1:p.Asn402=
NM_000488.4:c.1350C= MANE Select	NP_000479.1:p.Asn450=
NM_001365052.2:c.1206C=	NP_001351981.1:p.Asn402=
NM_001386302.1:c.1473C=	NP_001373231.1:p.Asn491=
NM_001386303.1:c.1431C=	NP_001373232.1:p.Asn477=
NM_001386304.1:c.1329C=	NP_001373233.1:p.Asn443=
NM_001386305.1:c.1293C=	NP_001373234.1:p.Asn431=
NM_001386306.1:c.1134C=	NP_001373235.1:p.Asn378=