Canonical Allele Identifier: CA1207936924
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909642A= , CM000663.2:g.173909642A= GRCh38
NC_000001.10:g.173878780A= , CM000663.1:g.173878780A= GRCh37
NC_000001.9:g.172145403A= NCBI36
NG_012462.1:g.12737T= , LRG_577:g.12737T=

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1063T= MANE Select ENSP00000356671.3:p.Phe355=
ENST00000367698.3:c.1063T= ENSP00000356671.3:p.Phe355=
ENST00000617423.4:c.560-2149T= ENSP00000478688.1:n.560-2149T=
NM_000488.3:c.1063T= , LRG_577t1:c.1063T= NP_000479.1:p.Phe355=
XM_005245198.2:c.919T= XP_005245255.1:p.Phe307=
NM_001365052.1:c.919T= NP_001351981.1:p.Phe307=
NM_000488.4:c.1063T= MANE Select NP_000479.1:p.Phe355=
NM_001365052.2:c.919T= NP_001351981.1:p.Phe307=
NM_001386302.1:c.1186T= NP_001373231.1:p.Phe396=
NM_001386303.1:c.1144T= NP_001373232.1:p.Phe382=
NM_001386304.1:c.1042T= NP_001373233.1:p.Phe348=
NM_001386305.1:c.1006T= NP_001373234.1:p.Phe336=
NM_001386306.1:c.847T= NP_001373235.1:p.Phe283=