Canonical Allele Identifier: CA1207936915
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909621_173909639delinsTGAAGCCGTCCTCAATGCG , CM000663.2:g.173909621_173909639delinsTGAAGCCGTCCTCAATGCG GRCh38
NC_000001.10:g.173878759_173878777delinsTGAAGCCGTCCTCAATGCG , CM000663.1:g.173878759_173878777delinsTGAAGCCGTCCTCAATGCG GRCh37
NC_000001.9:g.172145382_172145400delinsTGAAGCCGTCCTCAATGCG NCBI36
NG_012462.1:g.12740_12758delinsCGCATTGAGGACGGCTTCA , LRG_577:g.12740_12758delinsCGCATTGAGGACGGCTTCA

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1066_1084delinsCGCATTGAGGACGGCTTCA MANE Select ENSP00000356671.3:p.Arg356=
ENST00000367698.3:c.1066_1084delinsCGCATTGAGGACGGCTTCA ENSP00000356671.3:p.Arg356=
ENST00000617423.4:c.560-2146_560-2128delinsCGCATTGAGGACGGCTTCA ENSP00000478688.1:n.560-2146_560-2128deli...
NM_000488.3:c.1066_1084delinsCGCATTGAGGACGGCTTCA , LRG_577t1:c.1066_1084delinsCGCATTGAGGACGGCTTCA NP_000479.1:p.Arg356=
XM_005245198.2:c.922_940delinsCGCATTGAGGACGGCTTCA XP_005245255.1:p.Arg308=
NM_001365052.1:c.922_940delinsCGCATTGAGGACGGCTTCA NP_001351981.1:p.Arg308=
NM_000488.4:c.1066_1084delinsCGCATTGAGGACGGCTTCA MANE Select NP_000479.1:p.Arg356=
NM_001365052.2:c.922_940delinsCGCATTGAGGACGGCTTCA NP_001351981.1:p.Arg308=
NM_001386302.1:c.1189_1207delinsCGCATTGAGGACGGCTTCA NP_001373231.1:p.Arg397=
NM_001386303.1:c.1147_1165delinsCGCATTGAGGACGGCTTCA NP_001373232.1:p.Arg383=
NM_001386304.1:c.1045_1063delinsCGCATTGAGGACGGCTTCA NP_001373233.1:p.Arg349=
NM_001386305.1:c.1009_1027delinsCGCATTGAGGACGGCTTCA NP_001373234.1:p.Arg337=
NM_001386306.1:c.850_868delinsCGCATTGAGGACGGCTTCA NP_001373235.1:p.Arg284=