Canonical Allele Identifier: CA343773824
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878820A>T (hg19) chr1:g.173909682A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909682A>T , CM000663.2:g.173909682A>T GRCh38
NC_000001.10:g.173878820A>T , CM000663.1:g.173878820A>T GRCh37
NC_000001.9:g.172145443A>T NCBI36
NG_012462.1:g.12697T>A , LRG_577:g.12697T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1023T>A MANE Select ENSP00000356671.3:p.Asp341Glu
ENST00000367698.3:c.1023T>A ENSP00000356671.3:p.Asp341Glu
ENST00000617423.4:c.559+2182T>A ENSP00000478688.1:n.559+2182T>A
NM_000488.3:c.1023T>A , LRG_577t1:c.1023T>A NP_000479.1:p.Asp341Glu
XM_005245198.2:c.879T>A XP_005245255.1:p.Asp293Glu
NM_001365052.1:c.879T>A NP_001351981.1:p.Asp293Glu
NM_000488.4:c.1023T>A MANE Select NP_000479.1:p.Asp341Glu
NM_001365052.2:c.879T>A NP_001351981.1:p.Asp293Glu
NM_001386302.1:c.1146T>A NP_001373231.1:p.Asp382Glu
NM_001386303.1:c.1104T>A NP_001373232.1:p.Asp368Glu
NM_001386304.1:c.1002T>A NP_001373233.1:p.Asp334Glu
NM_001386305.1:c.966T>A NP_001373234.1:p.Asp322Glu
NM_001386306.1:c.807T>A NP_001373235.1:p.Asp269Glu
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