Canonical Allele Identifier: CA1207936971

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909736_173909738delinsGCT , CM000663.2:g.173909736_173909738delinsGCT	GRCh38
NC_000001.10:g.173878874_173878876delinsGCT , CM000663.1:g.173878874_173878876delinsGCT	GRCh37
NC_000001.9:g.172145497_172145499delinsGCT	NCBI36
NG_012462.1:g.12641_12643delinsAGC , LRG_577:g.12641_12643delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.967_969delinsAGC MANE Select	ENSP00000356671.3:p.Ser323=
ENST00000367698.3:c.967_969delinsAGC	ENSP00000356671.3:p.Ser323=
ENST00000487183.1:n.618_620delinsAGC
ENST00000617423.4:c.559+2126_559+2128delinsAGC	ENSP00000478688.1:n.559+2126_559+2128delinsAGC
NM_000488.3:c.967_969delinsAGC , LRG_577t1:c.967_969delinsAGC	NP_000479.1:p.Ser323=
XM_005245198.2:c.823_825delinsAGC	XP_005245255.1:p.Ser275=
NM_001365052.1:c.823_825delinsAGC	NP_001351981.1:p.Ser275=
NM_000488.4:c.967_969delinsAGC MANE Select	NP_000479.1:p.Ser323=
NM_001365052.2:c.823_825delinsAGC	NP_001351981.1:p.Ser275=
NM_001386302.1:c.1090_1092delinsAGC	NP_001373231.1:p.Ser364=
NM_001386303.1:c.1048_1050delinsAGC	NP_001373232.1:p.Ser350=
NM_001386304.1:c.946_948delinsAGC	NP_001373233.1:p.Ser316=
NM_001386305.1:c.910_912delinsAGC	NP_001373234.1:p.Ser304=
NM_001386306.1:c.751_753delinsAGC	NP_001373235.1:p.Ser251=