Canonical Allele Identifier: CA343773657
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909641A>T , CM000663.2:g.173909641A>T GRCh38
NC_000001.10:g.173878779A>T , CM000663.1:g.173878779A>T GRCh37
NC_000001.9:g.172145402A>T NCBI36
NG_012462.1:g.12738T>A , LRG_577:g.12738T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1064T>A MANE Select ENSP00000356671.3:p.Phe355Tyr
ENST00000367698.3:c.1064T>A ENSP00000356671.3:p.Phe355Tyr
ENST00000617423.4:c.560-2148T>A ENSP00000478688.1:n.560-2148T>A
NM_000488.3:c.1064T>A , LRG_577t1:c.1064T>A NP_000479.1:p.Phe355Tyr
XM_005245198.2:c.920T>A XP_005245255.1:p.Phe307Tyr
NM_001365052.1:c.920T>A NP_001351981.1:p.Phe307Tyr
NM_000488.4:c.1064T>A MANE Select NP_000479.1:p.Phe355Tyr
NM_001365052.2:c.920T>A NP_001351981.1:p.Phe307Tyr
NM_001386302.1:c.1187T>A NP_001373231.1:p.Phe396Tyr
NM_001386303.1:c.1145T>A NP_001373232.1:p.Phe382Tyr
NM_001386304.1:c.1043T>A NP_001373233.1:p.Phe348Tyr
NM_001386305.1:c.1007T>A NP_001373234.1:p.Phe336Tyr
NM_001386306.1:c.848T>A NP_001373235.1:p.Phe283Tyr