Canonical Allele Identifier: CA343772668
Gene: SERPINC1 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1234A>G MANE Select ENSP00000356671.3:p.Ser412Gly
ENST00000367698.3:c.1234A>G ENSP00000356671.3:p.Ser412Gly
ENST00000617423.4:c.619A>G ENSP00000478688.1:p.Ser207Gly
NM_000488.3:c.1234A>G , LRG_577t1:c.1234A>G NP_000479.1:p.Ser412Gly
XM_005245198.2:c.1090A>G XP_005245255.1:p.Ser364Gly
NM_001365052.1:c.1090A>G NP_001351981.1:p.Ser364Gly
NM_000488.4:c.1234A>G MANE Select NP_000479.1:p.Ser412Gly
NM_001365052.2:c.1090A>G NP_001351981.1:p.Ser364Gly
NM_001386302.1:c.1357A>G NP_001373231.1:p.Ser453Gly
NM_001386303.1:c.1315A>G NP_001373232.1:p.Ser439Gly
NM_001386304.1:c.1213A>G NP_001373233.1:p.Ser405Gly
NM_001386305.1:c.1177A>G NP_001373234.1:p.Ser393Gly
NM_001386306.1:c.1018A>G NP_001373235.1:p.Ser340Gly
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