Canonical Allele Identifier: CA343772027
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903900A>G , CM000663.2:g.173903900A>G GRCh38
NC_000001.10:g.173873038A>G , CM000663.1:g.173873038A>G GRCh37
NC_000001.9:g.172139661A>G NCBI36
NG_012462.1:g.18479T>C , LRG_577:g.18479T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1384T>C MANE Select ENSP00000356671.3:p.Cys462Arg
ENST00000367698.3:c.1384T>C ENSP00000356671.3:p.Cys462Arg
ENST00000617423.4:c.769T>C ENSP00000478688.1:p.Cys257Arg
NM_000488.3:c.1384T>C , LRG_577t1:c.1384T>C NP_000479.1:p.Cys462Arg
XM_005245198.2:c.1240T>C XP_005245255.1:p.Cys414Arg
NM_001365052.1:c.1240T>C NP_001351981.1:p.Cys414Arg
NM_000488.4:c.1384T>C MANE Select NP_000479.1:p.Cys462Arg
NM_001365052.2:c.1240T>C NP_001351981.1:p.Cys414Arg
NM_001386302.1:c.1507T>C NP_001373231.1:p.Cys503Arg
NM_001386303.1:c.1465T>C NP_001373232.1:p.Cys489Arg
NM_001386304.1:c.1363T>C NP_001373233.1:p.Cys455Arg
NM_001386305.1:c.1327T>C NP_001373234.1:p.Cys443Arg
NM_001386306.1:c.1168T>C NP_001373235.1:p.Cys390Arg