Canonical Allele Identifier: CA1207936954
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909691C= , CM000663.2:g.173909691C= GRCh38
NC_000001.10:g.173878829C= , CM000663.1:g.173878829C= GRCh37
NC_000001.9:g.172145452C= NCBI36
NG_012462.1:g.12688G= , LRG_577:g.12688G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1014G= MANE Select ENSP00000356671.3:p.Glu338=
ENST00000367698.3:c.1014G= ENSP00000356671.3:p.Glu338=
ENST00000617423.4:c.559+2173G= ENSP00000478688.1:n.559+2173G=
NM_000488.3:c.1014G= , LRG_577t1:c.1014G= NP_000479.1:p.Glu338=
XM_005245198.2:c.870G= XP_005245255.1:p.Glu290=
NM_001365052.1:c.870G= NP_001351981.1:p.Glu290=
NM_000488.4:c.1014G= MANE Select NP_000479.1:p.Glu338=
NM_001365052.2:c.870G= NP_001351981.1:p.Glu290=
NM_001386302.1:c.1137G= NP_001373231.1:p.Glu379=
NM_001386303.1:c.1095G= NP_001373232.1:p.Glu365=
NM_001386304.1:c.993G= NP_001373233.1:p.Glu331=
NM_001386305.1:c.957G= NP_001373234.1:p.Glu319=
NM_001386306.1:c.798G= NP_001373235.1:p.Glu266=