Canonical Allele Identifier: CA2586967709
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904011_173904013del , CM000663.2:g.173904011_173904013del GRCh38
NC_000001.10:g.173873149_173873151del , CM000663.1:g.173873149_173873151del GRCh37
NC_000001.9:g.172139772_172139774del NCBI36
NG_012462.1:g.18367_18369del , LRG_577:g.18367_18369del

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1272_1274del MANE Select ENSP00000356671.3:p.Arg425del
ENST00000367698.3:c.1272_1274del ENSP00000356671.3:p.Arg425del
ENST00000617423.4:c.657_659del ENSP00000478688.1:p.Arg220del
NM_000488.3:c.1272_1274del , LRG_577t1:c.1272_1274del NP_000479.1:p.Arg425del
XM_005245198.2:c.1128_1130del XP_005245255.1:p.Arg377del
NM_001365052.1:c.1128_1130del NP_001351981.1:p.Arg377del
NM_000488.4:c.1272_1274del MANE Select NP_000479.1:p.Arg425del
NM_001365052.2:c.1128_1130del NP_001351981.1:p.Arg377del
NM_001386302.1:c.1395_1397del NP_001373231.1:p.Arg466del
NM_001386303.1:c.1353_1355del NP_001373232.1:p.Arg452del
NM_001386304.1:c.1251_1253del NP_001373233.1:p.Arg418del
NM_001386305.1:c.1215_1217del NP_001373234.1:p.Arg406del
NM_001386306.1:c.1056_1058del NP_001373235.1:p.Arg353del