Canonical Allele Identifier: CA2582343015
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903963_173903964insT , CM000663.2:g.173903963_173903964insT GRCh38
NC_000001.10:g.173873101_173873102insT , CM000663.1:g.173873101_173873102insT GRCh37
NC_000001.9:g.172139724_172139725insT NCBI36
NG_012462.1:g.18415_18416insA , LRG_577:g.18415_18416insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1320_1321insA MANE Select ENSP00000356671.3:p.Leu441ThrfsTer24
ENST00000367698.3:c.1320_1321insA ENSP00000356671.3:p.Leu441ThrfsTer24
ENST00000617423.4:c.705_706insA ENSP00000478688.1:p.Leu236ThrfsTer24
NM_000488.3:c.1320_1321insA , LRG_577t1:c.1320_1321insA NP_000479.1:p.Leu441ThrfsTer24
XM_005245198.2:c.1176_1177insA XP_005245255.1:p.Leu393ThrfsTer24
NM_001365052.1:c.1176_1177insA NP_001351981.1:p.Leu393ThrfsTer24
NM_000488.4:c.1320_1321insA MANE Select NP_000479.1:p.Leu441ThrfsTer24
NM_001365052.2:c.1176_1177insA NP_001351981.1:p.Leu393ThrfsTer24
NM_001386302.1:c.1443_1444insA NP_001373231.1:p.Leu482ThrfsTer24
NM_001386303.1:c.1401_1402insA NP_001373232.1:p.Leu468ThrfsTer24
NM_001386304.1:c.1299_1300insA NP_001373233.1:p.Leu434ThrfsTer24
NM_001386305.1:c.1263_1264insA NP_001373234.1:p.Leu422ThrfsTer24
NM_001386306.1:c.1104_1105insA NP_001373235.1:p.Leu369ThrfsTer24