Canonical Allele Identifier: CA2580060415
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903908del , CM000663.2:g.173903908del GRCh38
NC_000001.10:g.173873046del , CM000663.1:g.173873046del GRCh37
NC_000001.9:g.172139669del NCBI36
NG_012462.1:g.18472del , LRG_577:g.18472del

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1377del MANE Select ENSP00000356671.3:p.Asn460ThrfsTer20
ENST00000367698.3:c.1377del ENSP00000356671.3:p.Asn460ThrfsTer20
ENST00000617423.4:c.762del ENSP00000478688.1:p.Asn255ThrfsTer20
NM_000488.3:c.1377del , LRG_577t1:c.1377del NP_000479.1:p.Asn460ThrfsTer20
XM_005245198.2:c.1233del XP_005245255.1:p.Asn412ThrfsTer20
NM_001365052.1:c.1233del NP_001351981.1:p.Asn412ThrfsTer20
NM_000488.4:c.1377del MANE Select NP_000479.1:p.Asn460ThrfsTer20
NM_001365052.2:c.1233del NP_001351981.1:p.Asn412ThrfsTer20
NM_001386302.1:c.1500del NP_001373231.1:p.Asn501ThrfsTer20
NM_001386303.1:c.1458del NP_001373232.1:p.Asn487ThrfsTer20
NM_001386304.1:c.1356del NP_001373233.1:p.Asn453ThrfsTer20
NM_001386305.1:c.1320del NP_001373234.1:p.Asn441ThrfsTer20
NM_001386306.1:c.1161del NP_001373235.1:p.Asn388ThrfsTer20