Canonical Allele Identifier: CA343772133
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1359392415

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903923A>C , CM000663.2:g.173903923A>C GRCh38
NC_000001.10:g.173873061A>C , CM000663.1:g.173873061A>C GRCh37
NC_000001.9:g.172139684A>C NCBI36
NG_012462.1:g.18456T>G , LRG_577:g.18456T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1361T>G MANE Select ENSP00000356671.3:p.Phe454Cys
ENST00000367698.3:c.1361T>G ENSP00000356671.3:p.Phe454Cys
ENST00000617423.4:c.746T>G ENSP00000478688.1:p.Phe249Cys
NM_000488.3:c.1361T>G , LRG_577t1:c.1361T>G NP_000479.1:p.Phe454Cys
XM_005245198.2:c.1217T>G XP_005245255.1:p.Phe406Cys
NM_001365052.1:c.1217T>G NP_001351981.1:p.Phe406Cys
NM_000488.4:c.1361T>G MANE Select NP_000479.1:p.Phe454Cys
NM_001365052.2:c.1217T>G NP_001351981.1:p.Phe406Cys
NM_001386302.1:c.1484T>G NP_001373231.1:p.Phe495Cys
NM_001386303.1:c.1442T>G NP_001373232.1:p.Phe481Cys
NM_001386304.1:c.1340T>G NP_001373233.1:p.Phe447Cys
NM_001386305.1:c.1304T>G NP_001373234.1:p.Phe435Cys
NM_001386306.1:c.1145T>G NP_001373235.1:p.Phe382Cys