Canonical Allele Identifier: CA1207938928

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173914596G= , CM000663.2:g.173914596G=	GRCh38
NC_000001.10:g.173883734G= , CM000663.1:g.173883734G=	GRCh37
NC_000001.9:g.172150357G=	NCBI36
NG_012462.1:g.7783C= , LRG_577:g.7783C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.365C= MANE Select	ENSP00000356671.3:p.Thr122=
ENST00000367698.3:c.365C=	ENSP00000356671.3:p.Thr122=
ENST00000487183.1:n.70C=
ENST00000494024.1:n.591C=
ENST00000617423.4:c.365C=	ENSP00000478688.1:p.Thr122=
NM_000488.3:c.365C= , LRG_577t1:c.365C=	NP_000479.1:p.Thr122=
XM_005245198.2:c.221C=	XP_005245255.1:p.Thr74=
NM_001365052.1:c.221C=	NP_001351981.1:p.Thr74=
NM_000488.4:c.365C= MANE Select	NP_000479.1:p.Thr122=
NM_001365052.2:c.221C=	NP_001351981.1:p.Thr74=
NM_001386302.1:c.365C=	NP_001373231.1:p.Thr122=
NM_001386303.1:c.446C=	NP_001373232.1:p.Thr149=
NM_001386304.1:c.365C=	NP_001373233.1:p.Thr122=
NM_001386305.1:c.365C=	NP_001373234.1:p.Thr122=
NM_001386306.1:c.365C=	NP_001373235.1:p.Thr122=