Canonical Allele Identifier: CA1207936996

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909792G= , CM000663.2:g.173909792G=	GRCh38
NC_000001.10:g.173878930G= , CM000663.1:g.173878930G=	GRCh37
NC_000001.9:g.172145553G=	NCBI36
NG_012462.1:g.12587C= , LRG_577:g.12587C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.913C= MANE Select	ENSP00000356671.3:p.Pro305=
ENST00000367698.3:c.913C=	ENSP00000356671.3:p.Pro305=
ENST00000487183.1:n.564C=
ENST00000617423.4:c.559+2072C=	ENSP00000478688.1:n.559+2072C=
NM_000488.3:c.913C= , LRG_577t1:c.913C=	NP_000479.1:p.Pro305=
XM_005245198.2:c.769C=	XP_005245255.1:p.Pro257=
NM_001365052.1:c.769C=	NP_001351981.1:p.Pro257=
NM_000488.4:c.913C= MANE Select	NP_000479.1:p.Pro305=
NM_001365052.2:c.769C=	NP_001351981.1:p.Pro257=
NM_001386302.1:c.1036C=	NP_001373231.1:p.Pro346=
NM_001386303.1:c.994C=	NP_001373232.1:p.Pro332=
NM_001386304.1:c.892C=	NP_001373233.1:p.Pro298=
NM_001386305.1:c.856C=	NP_001373234.1:p.Pro286=
NM_001386306.1:c.697C=	NP_001373235.1:p.Pro233=