Canonical Allele Identifier: CA343773876
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878831C>T (hg19) chr1:g.173909693C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909693C>T , CM000663.2:g.173909693C>T GRCh38
NC_000001.10:g.173878831C>T , CM000663.1:g.173878831C>T GRCh37
NC_000001.9:g.172145454C>T NCBI36
NG_012462.1:g.12686G>A , LRG_577:g.12686G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1012G>A MANE Select ENSP00000356671.3:p.Glu338Lys
ENST00000367698.3:c.1012G>A ENSP00000356671.3:p.Glu338Lys
ENST00000617423.4:c.559+2171G>A ENSP00000478688.1:n.559+2171G>A
NM_000488.3:c.1012G>A , LRG_577t1:c.1012G>A NP_000479.1:p.Glu338Lys
XM_005245198.2:c.868G>A XP_005245255.1:p.Glu290Lys
NM_001365052.1:c.868G>A NP_001351981.1:p.Glu290Lys
NM_000488.4:c.1012G>A MANE Select NP_000479.1:p.Glu338Lys
NM_001365052.2:c.868G>A NP_001351981.1:p.Glu290Lys
NM_001386302.1:c.1135G>A NP_001373231.1:p.Glu379Lys
NM_001386303.1:c.1093G>A NP_001373232.1:p.Glu365Lys
NM_001386304.1:c.991G>A NP_001373233.1:p.Glu331Lys
NM_001386305.1:c.955G>A NP_001373234.1:p.Glu319Lys
NM_001386306.1:c.796G>A NP_001373235.1:p.Glu266Lys
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