Canonical Allele Identifier: CA2560111250
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903882_173903884del , CM000663.2:g.173903882_173903884del GRCh38
NC_000001.10:g.173873020_173873022del , CM000663.1:g.173873020_173873022del GRCh37
NC_000001.9:g.172139643_172139645del NCBI36
NG_012462.1:g.18497_18499del , LRG_577:g.18497_18499del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.*7_*9del MANE Select ENSP00000356671.3:n.*7_*9del
ENST00000367698.3:c.*7_*9del ENSP00000356671.3:n.*7_*9del
ENST00000617423.4:c.*7_*9del ENSP00000478688.1:n.*7_*9del
NM_000488.3:c.*7_*9del , LRG_577t1:c.*7_*9del NP_000479.1:n.*7_*9del
XM_005245198.2:c.*7_*9del XP_005245255.1:n.*7_*9del
NM_001365052.1:c.*7_*9del NP_001351981.1:n.*7_*9del
NM_000488.4:c.*7_*9del MANE Select NP_000479.1:n.*7_*9del
NM_001365052.2:c.*7_*9del NP_001351981.1:n.*7_*9del
NM_001386302.1:c.*7_*9del NP_001373231.1:n.*7_*9del
NM_001386303.1:c.*7_*9del NP_001373232.1:n.*7_*9del
NM_001386304.1:c.*7_*9del NP_001373233.1:n.*7_*9del
NM_001386305.1:c.*7_*9del NP_001373234.1:n.*7_*9del
NM_001386306.1:c.*7_*9del NP_001373235.1:n.*7_*9del