Canonical Allele Identifier: CA1207939935

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173917204G= , CM000663.2:g.173917204G=	GRCh38
NC_000001.10:g.173886342G= , CM000663.1:g.173886342G=	GRCh37
NC_000001.9:g.172152965G=	NCBI36
NG_012462.1:g.5175C= , LRG_577:g.5175C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.41+15C= MANE Select	ENSP00000356671.3:n.41+15C=
ENST00000367698.3:c.41+15C=	ENSP00000356671.3:n.41+15C=
ENST00000494024.1:n.98+15C=
ENST00000617423.4:c.41+15C=	ENSP00000478688.1:n.41+15C=
NM_000488.3:c.41+15C= , LRG_577t1:c.41+15C=	NP_000479.1:n.41+15C=
XM_005245198.2:c.-273+15C=	XP_005245255.1:n.-273+15C=
NM_001365052.1:c.-273+15C=	NP_001351981.1:n.-273+15C=
NM_000488.4:c.41+15C= MANE Select	NP_000479.1:n.41+15C=
NM_001365052.2:c.-273+15C=	NP_001351981.1:n.-273+15C=
NM_001386302.1:c.41+15C=	NP_001373231.1:n.41+15C=
NM_001386303.1:c.24+32C=	NP_001373232.1:n.24+32C=
NM_001386304.1:c.41+15C=	NP_001373233.1:n.41+15C=
NM_001386305.1:c.41+15C=	NP_001373234.1:n.41+15C=
NM_001386306.1:c.41+15C=	NP_001373235.1:n.41+15C=