Canonical Allele Identifier: CA2586967698

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903916_173903917delinsTGTAG , CM000663.2:g.173903916_173903917delinsTGTAG	GRCh38
NC_000001.10:g.173873054_173873055delinsTGTAG , CM000663.1:g.173873054_173873055delinsTGTAG	GRCh37
NC_000001.9:g.172139677_172139678delinsTGTAG	NCBI36
NG_012462.1:g.18462_18463delinsCTACA , LRG_577:g.18462_18463delinsCTACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1367_1368delinsCTACA MANE Select	ENSP00000356671.3:p.Gly456delinsAlaThr
ENST00000367698.3:c.1367_1368delinsCTACA	ENSP00000356671.3:p.Gly456delinsAlaThr
ENST00000617423.4:c.752_753delinsCTACA	ENSP00000478688.1:p.Gly251delinsAlaThr
NM_000488.3:c.1367_1368delinsCTACA , LRG_577t1:c.1367_1368delinsCTACA	NP_000479.1:p.Gly456delinsAlaThr
XM_005245198.2:c.1223_1224delinsCTACA	XP_005245255.1:p.Gly408delinsAlaThr
NM_001365052.1:c.1223_1224delinsCTACA	NP_001351981.1:p.Gly408delinsAlaThr
NM_000488.4:c.1367_1368delinsCTACA MANE Select	NP_000479.1:p.Gly456delinsAlaThr
NM_001365052.2:c.1223_1224delinsCTACA	NP_001351981.1:p.Gly408delinsAlaThr
NM_001386302.1:c.1490_1491delinsCTACA	NP_001373231.1:p.Gly497delinsAlaThr
NM_001386303.1:c.1448_1449delinsCTACA	NP_001373232.1:p.Gly483delinsAlaThr
NM_001386304.1:c.1346_1347delinsCTACA	NP_001373233.1:p.Gly449delinsAlaThr
NM_001386305.1:c.1310_1311delinsCTACA	NP_001373234.1:p.Gly437delinsAlaThr
NM_001386306.1:c.1151_1152delinsCTACA	NP_001373235.1:p.Gly384delinsAlaThr