Canonical Allele Identifier: CA2586964409
Gene: SERPINC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909919del , CM000663.2:g.173909919del GRCh38
NC_000001.10:g.173879057del , CM000663.1:g.173879057del GRCh37
NC_000001.9:g.172145680del NCBI36
NG_012462.1:g.12462del , LRG_577:g.12462del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.788del MANE Select ENSP00000356671.3:p.Pro263LeufsTer21
ENST00000367698.3:c.788del ENSP00000356671.3:p.Pro263LeufsTer21
ENST00000487183.1:n.439del
ENST00000617423.4:c.559+1947del ENSP00000478688.1:n.559+1947del
NM_000488.3:c.788del , LRG_577t1:c.788del NP_000479.1:p.Pro263LeufsTer21
XM_005245198.2:c.644del XP_005245255.1:p.Pro215LeufsTer21
NM_001365052.1:c.644del NP_001351981.1:p.Pro215LeufsTer21
NM_000488.4:c.788del MANE Select NP_000479.1:p.Pro263LeufsTer21
NM_001365052.2:c.644del NP_001351981.1:p.Pro215LeufsTer21
NM_001386302.1:c.911del NP_001373231.1:p.Pro304LeufsTer21
NM_001386303.1:c.869del NP_001373232.1:p.Pro290LeufsTer21
NM_001386304.1:c.767del NP_001373233.1:p.Pro256LeufsTer21
NM_001386305.1:c.763-32del NP_001373234.1:n.763-32del
NM_001386306.1:c.572del NP_001373235.1:p.Pro191LeufsTer21
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