Canonical Allele Identifier: CA2586967705
Gene: SERPINC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903964_173903965insT , CM000663.2:g.173903964_173903965insT GRCh38
NC_000001.10:g.173873102_173873103insT , CM000663.1:g.173873102_173873103insT GRCh37
NC_000001.9:g.172139725_172139726insT NCBI36
NG_012462.1:g.18414_18415insA , LRG_577:g.18414_18415insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1319_1320insA MANE Select ENSP00000356671.3:p.Phe440LeufsTer25
ENST00000367698.3:c.1319_1320insA ENSP00000356671.3:p.Phe440LeufsTer25
ENST00000617423.4:c.704_705insA ENSP00000478688.1:p.Phe235LeufsTer25
NM_000488.3:c.1319_1320insA , LRG_577t1:c.1319_1320insA NP_000479.1:p.Phe440LeufsTer25
XM_005245198.2:c.1175_1176insA XP_005245255.1:p.Phe392LeufsTer25
NM_001365052.1:c.1175_1176insA NP_001351981.1:p.Phe392LeufsTer25
NM_000488.4:c.1319_1320insA MANE Select NP_000479.1:p.Phe440LeufsTer25
NM_001365052.2:c.1175_1176insA NP_001351981.1:p.Phe392LeufsTer25
NM_001386302.1:c.1442_1443insA NP_001373231.1:p.Phe481LeufsTer25
NM_001386303.1:c.1400_1401insA NP_001373232.1:p.Phe467LeufsTer25
NM_001386304.1:c.1298_1299insA NP_001373233.1:p.Phe433LeufsTer25
NM_001386305.1:c.1262_1263insA NP_001373234.1:p.Phe421LeufsTer25
NM_001386306.1:c.1103_1104insA NP_001373235.1:p.Phe368LeufsTer25
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