Canonical Allele Identifier: CA343772666
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873188T>G (hg19) chr1:g.173904050T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904050T>G , CM000663.2:g.173904050T>G GRCh38
NC_000001.10:g.173873188T>G , CM000663.1:g.173873188T>G GRCh37
NC_000001.9:g.172139811T>G NCBI36
NG_012462.1:g.18329A>C , LRG_577:g.18329A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1234A>C MANE Select ENSP00000356671.3:p.Ser412Arg
ENST00000367698.3:c.1234A>C ENSP00000356671.3:p.Ser412Arg
ENST00000617423.4:c.619A>C ENSP00000478688.1:p.Ser207Arg
NM_000488.3:c.1234A>C , LRG_577t1:c.1234A>C NP_000479.1:p.Ser412Arg
XM_005245198.2:c.1090A>C XP_005245255.1:p.Ser364Arg
NM_001365052.1:c.1090A>C NP_001351981.1:p.Ser364Arg
NM_000488.4:c.1234A>C MANE Select NP_000479.1:p.Ser412Arg
NM_001365052.2:c.1090A>C NP_001351981.1:p.Ser364Arg
NM_001386302.1:c.1357A>C NP_001373231.1:p.Ser453Arg
NM_001386303.1:c.1315A>C NP_001373232.1:p.Ser439Arg
NM_001386304.1:c.1213A>C NP_001373233.1:p.Ser405Arg
NM_001386305.1:c.1177A>C NP_001373234.1:p.Ser393Arg
NM_001386306.1:c.1018A>C NP_001373235.1:p.Ser340Arg
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