Canonical Allele Identifier: CA2582342991
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903901_173903909del , CM000663.2:g.173903901_173903909del GRCh38
NC_000001.10:g.173873039_173873047del , CM000663.1:g.173873039_173873047del GRCh37
NC_000001.9:g.172139662_172139670del NCBI36
NG_012462.1:g.18470_18478del , LRG_577:g.18470_18478del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1375_1383del MANE Select ENSP00000356671.3:p.Ala459_Pro461del
ENST00000367698.3:c.1375_1383del ENSP00000356671.3:p.Ala459_Pro461del
ENST00000617423.4:c.760_768del ENSP00000478688.1:p.Ala254_Pro256del
NM_000488.3:c.1375_1383del , LRG_577t1:c.1375_1383del NP_000479.1:p.Ala459_Pro461del
XM_005245198.2:c.1231_1239del XP_005245255.1:p.Ala411_Pro413del
NM_001365052.1:c.1231_1239del NP_001351981.1:p.Ala411_Pro413del
NM_000488.4:c.1375_1383del MANE Select NP_000479.1:p.Ala459_Pro461del
NM_001365052.2:c.1231_1239del NP_001351981.1:p.Ala411_Pro413del
NM_001386302.1:c.1498_1506del NP_001373231.1:p.Ala500_Pro502del
NM_001386303.1:c.1456_1464del NP_001373232.1:p.Ala486_Pro488del
NM_001386304.1:c.1354_1362del NP_001373233.1:p.Ala452_Pro454del
NM_001386305.1:c.1318_1326del NP_001373234.1:p.Ala440_Pro442del
NM_001386306.1:c.1159_1167del NP_001373235.1:p.Ala387_Pro389del