Canonical Allele Identifier: CA343773770
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878808C>G (hg19) chr1:g.173909670C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909670C>G , CM000663.2:g.173909670C>G GRCh38
NC_000001.10:g.173878808C>G , CM000663.1:g.173878808C>G GRCh37
NC_000001.9:g.172145431C>G NCBI36
NG_012462.1:g.12709G>C , LRG_577:g.12709G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1035G>C MANE Select ENSP00000356671.3:p.Glu345Asp
ENST00000367698.3:c.1035G>C ENSP00000356671.3:p.Glu345Asp
ENST00000617423.4:c.560-2177G>C ENSP00000478688.1:n.560-2177G>C
NM_000488.3:c.1035G>C , LRG_577t1:c.1035G>C NP_000479.1:p.Glu345Asp
XM_005245198.2:c.891G>C XP_005245255.1:p.Glu297Asp
NM_001365052.1:c.891G>C NP_001351981.1:p.Glu297Asp
NM_000488.4:c.1035G>C MANE Select NP_000479.1:p.Glu345Asp
NM_001365052.2:c.891G>C NP_001351981.1:p.Glu297Asp
NM_001386302.1:c.1158G>C NP_001373231.1:p.Glu386Asp
NM_001386303.1:c.1116G>C NP_001373232.1:p.Glu372Asp
NM_001386304.1:c.1014G>C NP_001373233.1:p.Glu338Asp
NM_001386305.1:c.978G>C NP_001373234.1:p.Glu326Asp
NM_001386306.1:c.819G>C NP_001373235.1:p.Glu273Asp
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