Canonical Allele Identifier: CA1207939839
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1658017673

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173916982_173916986del , CM000663.2:g.173916982_173916986del GRCh38
NC_000001.10:g.173886120_173886124del , CM000663.1:g.173886120_173886124del GRCh37
NC_000001.9:g.172152743_172152747del NCBI36
NG_012462.1:g.5395_5399del , LRG_577:g.5395_5399del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.41+235_41+239del MANE Select ENSP00000356671.3:n.41+235_41+239del
ENST00000367698.3:c.41+235_41+239del ENSP00000356671.3:n.41+235_41+239del
ENST00000494024.1:n.98+235_98+239del
ENST00000617423.4:c.41+235_41+239del ENSP00000478688.1:n.41+235_41+239del
NM_000488.3:c.41+235_41+239del , LRG_577t1:c.41+235_41+239del NP_000479.1:n.41+235_41+239del
XM_005245198.2:c.-273+235_-273+239del XP_005245255.1:n.-273+235_-273+239del
NM_001365052.1:c.-273+235_-273+239del NP_001351981.1:n.-273+235_-273+239del
NM_000488.4:c.41+235_41+239del MANE Select NP_000479.1:n.41+235_41+239del
NM_001365052.2:c.-273+235_-273+239del NP_001351981.1:n.-273+235_-273+239del
NM_001386302.1:c.41+235_41+239del NP_001373231.1:n.41+235_41+239del
NM_001386303.1:c.24+252_24+256del NP_001373232.1:n.24+252_24+256del
NM_001386304.1:c.41+235_41+239del NP_001373233.1:n.41+235_41+239del
NM_001386305.1:c.41+235_41+239del NP_001373234.1:n.41+235_41+239del
NM_001386306.1:c.41+235_41+239del NP_001373235.1:n.41+235_41+239del