Canonical Allele Identifier: CA2586964428

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911985_173911990delinsATTCTA , CM000663.2:g.173911985_173911990delinsATTCTA	GRCh38
NC_000001.10:g.173881123_173881128delinsATTCTA , CM000663.1:g.173881123_173881128delinsATTCTA	GRCh37
NC_000001.9:g.172147746_172147751delinsATTCTA	NCBI36
NG_012462.1:g.10389_10394delinsTAGAAT , LRG_577:g.10389_10394delinsTAGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.433_438delinsTAGAAT MANE Select	ENSP00000356671.3:p.Glu145Ter
ENST00000367698.3:c.433_438delinsTAGAAT	ENSP00000356671.3:p.Glu145Ter
ENST00000487183.1:n.138_143delinsTAGAAT
ENST00000494024.1:n.659_664delinsTAGAAT
ENST00000617423.4:c.433_438delinsTAGAAT	ENSP00000478688.1:p.Glu145Ter
NM_000488.3:c.433_438delinsTAGAAT , LRG_577t1:c.433_438delinsTAGAAT	NP_000479.1:p.Glu145Ter
XM_005245198.2:c.289_294delinsTAGAAT	XP_005245255.1:p.Glu97Ter
NM_001365052.1:c.289_294delinsTAGAAT	NP_001351981.1:p.Glu97Ter
NM_000488.4:c.433_438delinsTAGAAT MANE Select	NP_000479.1:p.Glu145Ter
NM_001365052.2:c.289_294delinsTAGAAT	NP_001351981.1:p.Glu97Ter
NM_001386302.1:c.433_438delinsTAGAAT	NP_001373231.1:p.Glu145Ter
NM_001386303.1:c.514_519delinsTAGAAT	NP_001373232.1:p.Glu172Ter
NM_001386304.1:c.433_438delinsTAGAAT	NP_001373233.1:p.Glu145Ter
NM_001386305.1:c.433_438delinsTAGAAT	NP_001373234.1:p.Glu145Ter
NM_001386306.1:c.409-1099_409-1094delinsTAGAAT	NP_001373235.1:n.409-1099_409-1094delinsTAGAAT