Canonical Allele Identifier: CA1207936936
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909663G= , CM000663.2:g.173909663G= GRCh38
NC_000001.10:g.173878801G= , CM000663.1:g.173878801G= GRCh37
NC_000001.9:g.172145424G= NCBI36
NG_012462.1:g.12716C= , LRG_577:g.12716C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1042C= MANE Select ENSP00000356671.3:p.Leu348=
ENST00000367698.3:c.1042C= ENSP00000356671.3:p.Leu348=
ENST00000617423.4:c.560-2170C= ENSP00000478688.1:n.560-2170C=
NM_000488.3:c.1042C= , LRG_577t1:c.1042C= NP_000479.1:p.Leu348=
XM_005245198.2:c.898C= XP_005245255.1:p.Leu300=
NM_001365052.1:c.898C= NP_001351981.1:p.Leu300=
NM_000488.4:c.1042C= MANE Select NP_000479.1:p.Leu348=
NM_001365052.2:c.898C= NP_001351981.1:p.Leu300=
NM_001386302.1:c.1165C= NP_001373231.1:p.Leu389=
NM_001386303.1:c.1123C= NP_001373232.1:p.Leu375=
NM_001386304.1:c.1021C= NP_001373233.1:p.Leu341=
NM_001386305.1:c.985C= NP_001373234.1:p.Leu329=
NM_001386306.1:c.826C= NP_001373235.1:p.Leu276=