Canonical Allele Identifier: CA343773732
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878801G>T (hg19) chr1:g.173909663G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909663G>T , CM000663.2:g.173909663G>T GRCh38
NC_000001.10:g.173878801G>T , CM000663.1:g.173878801G>T GRCh37
NC_000001.9:g.172145424G>T NCBI36
NG_012462.1:g.12716C>A , LRG_577:g.12716C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1042C>A MANE Select ENSP00000356671.3:p.Leu348Met
ENST00000367698.3:c.1042C>A ENSP00000356671.3:p.Leu348Met
ENST00000617423.4:c.560-2170C>A ENSP00000478688.1:n.560-2170C>A
NM_000488.3:c.1042C>A , LRG_577t1:c.1042C>A NP_000479.1:p.Leu348Met
XM_005245198.2:c.898C>A XP_005245255.1:p.Leu300Met
NM_001365052.1:c.898C>A NP_001351981.1:p.Leu300Met
NM_000488.4:c.1042C>A MANE Select NP_000479.1:p.Leu348Met
NM_001365052.2:c.898C>A NP_001351981.1:p.Leu300Met
NM_001386302.1:c.1165C>A NP_001373231.1:p.Leu389Met
NM_001386303.1:c.1123C>A NP_001373232.1:p.Leu375Met
NM_001386304.1:c.1021C>A NP_001373233.1:p.Leu341Met
NM_001386305.1:c.985C>A NP_001373234.1:p.Leu329Met
NM_001386306.1:c.826C>A NP_001373235.1:p.Leu276Met
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