Canonical Allele Identifier: CA343774724
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879036T>G (hg19) chr1:g.173909898T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909898T>G , CM000663.2:g.173909898T>G GRCh38
NC_000001.10:g.173879036T>G , CM000663.1:g.173879036T>G GRCh37
NC_000001.9:g.172145659T>G NCBI36
NG_012462.1:g.12481A>C , LRG_577:g.12481A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.807A>C MANE Select ENSP00000356671.3:p.Glu269Asp
ENST00000367698.3:c.807A>C ENSP00000356671.3:p.Glu269Asp
ENST00000487183.1:n.458A>C
ENST00000617423.4:c.559+1966A>C ENSP00000478688.1:n.559+1966A>C
NM_000488.3:c.807A>C , LRG_577t1:c.807A>C NP_000479.1:p.Glu269Asp
XM_005245198.2:c.663A>C XP_005245255.1:p.Glu221Asp
NM_001365052.1:c.663A>C NP_001351981.1:p.Glu221Asp
NM_000488.4:c.807A>C MANE Select NP_000479.1:p.Glu269Asp
NM_001365052.2:c.663A>C NP_001351981.1:p.Glu221Asp
NM_001386302.1:c.930A>C NP_001373231.1:p.Glu310Asp
NM_001386303.1:c.888A>C NP_001373232.1:p.Glu296Asp
NM_001386304.1:c.786A>C NP_001373233.1:p.Glu262Asp
NM_001386305.1:c.763-13A>C NP_001373234.1:n.763-13A>C
NM_001386306.1:c.591A>C NP_001373235.1:p.Glu197Asp
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