Canonical Allele Identifier: CA1207936958

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909714G= , CM000663.2:g.173909714G=	GRCh38
NC_000001.10:g.173878852G= , CM000663.1:g.173878852G=	GRCh37
NC_000001.9:g.172145475G=	NCBI36
NG_012462.1:g.12665C= , LRG_577:g.12665C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.991C= MANE Select	ENSP00000356671.3:p.Leu331=
ENST00000367698.3:c.991C=	ENSP00000356671.3:p.Leu331=
ENST00000617423.4:c.559+2150C=	ENSP00000478688.1:n.559+2150C=
NM_000488.3:c.991C= , LRG_577t1:c.991C=	NP_000479.1:p.Leu331=
XM_005245198.2:c.847C=	XP_005245255.1:p.Leu283=
NM_001365052.1:c.847C=	NP_001351981.1:p.Leu283=
NM_000488.4:c.991C= MANE Select	NP_000479.1:p.Leu331=
NM_001365052.2:c.847C=	NP_001351981.1:p.Leu283=
NM_001386302.1:c.1114C=	NP_001373231.1:p.Leu372=
NM_001386303.1:c.1072C=	NP_001373232.1:p.Leu358=
NM_001386304.1:c.970C=	NP_001373233.1:p.Leu324=
NM_001386305.1:c.934C=	NP_001373234.1:p.Leu312=
NM_001386306.1:c.775C=	NP_001373235.1:p.Leu259=