Canonical Allele Identifier: CA343774785
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879062A>C (hg19) chr1:g.173909924A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909924A>C , CM000663.2:g.173909924A>C GRCh38
NC_000001.10:g.173879062A>C , CM000663.1:g.173879062A>C GRCh37
NC_000001.9:g.172145685A>C NCBI36
NG_012462.1:g.12455T>G , LRG_577:g.12455T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.781T>G MANE Select ENSP00000356671.3:p.Phe261Val
ENST00000367698.3:c.781T>G ENSP00000356671.3:p.Phe261Val
ENST00000487183.1:n.432T>G
ENST00000617423.4:c.559+1940T>G ENSP00000478688.1:n.559+1940T>G
NM_000488.3:c.781T>G , LRG_577t1:c.781T>G NP_000479.1:p.Phe261Val
XM_005245198.2:c.637T>G XP_005245255.1:p.Phe213Val
NM_001365052.1:c.637T>G NP_001351981.1:p.Phe213Val
NM_000488.4:c.781T>G MANE Select NP_000479.1:p.Phe261Val
NM_001365052.2:c.637T>G NP_001351981.1:p.Phe213Val
NM_001386302.1:c.904T>G NP_001373231.1:p.Phe302Val
NM_001386303.1:c.862T>G NP_001373232.1:p.Phe288Val
NM_001386304.1:c.760T>G NP_001373233.1:p.Phe254Val
NM_001386305.1:c.763-39T>G NP_001373234.1:n.763-39T>G
NM_001386306.1:c.565T>G NP_001373235.1:p.Phe189Val
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