Canonical Allele Identifier: CA343774424
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878968T>C (hg19) chr1:g.173909830T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909830T>C , CM000663.2:g.173909830T>C GRCh38
NC_000001.10:g.173878968T>C , CM000663.1:g.173878968T>C GRCh37
NC_000001.9:g.172145591T>C NCBI36
NG_012462.1:g.12549A>G , LRG_577:g.12549A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.875A>G MANE Select ENSP00000356671.3:p.Tyr292Cys
ENST00000367698.3:c.875A>G ENSP00000356671.3:p.Tyr292Cys
ENST00000487183.1:n.526A>G
ENST00000617423.4:c.559+2034A>G ENSP00000478688.1:n.559+2034A>G
NM_000488.3:c.875A>G , LRG_577t1:c.875A>G NP_000479.1:p.Tyr292Cys
XM_005245198.2:c.731A>G XP_005245255.1:p.Tyr244Cys
NM_001365052.1:c.731A>G NP_001351981.1:p.Tyr244Cys
NM_000488.4:c.875A>G MANE Select NP_000479.1:p.Tyr292Cys
NM_001365052.2:c.731A>G NP_001351981.1:p.Tyr244Cys
NM_001386302.1:c.998A>G NP_001373231.1:p.Tyr333Cys
NM_001386303.1:c.956A>G NP_001373232.1:p.Tyr319Cys
NM_001386304.1:c.854A>G NP_001373233.1:p.Tyr285Cys
NM_001386305.1:c.818A>G NP_001373234.1:p.Tyr273Cys
NM_001386306.1:c.659A>G NP_001373235.1:p.Tyr220Cys
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