Canonical Allele Identifier: CA343772624
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873166G>T (hg19) chr1:g.173904028G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904028G>T , CM000663.2:g.173904028G>T GRCh38
NC_000001.10:g.173873166G>T , CM000663.1:g.173873166G>T GRCh37
NC_000001.9:g.172139789G>T NCBI36
NG_012462.1:g.18351C>A , LRG_577:g.18351C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1256C>A MANE Select ENSP00000356671.3:p.Ala419Asp
ENST00000367698.3:c.1256C>A ENSP00000356671.3:p.Ala419Asp
ENST00000617423.4:c.641C>A ENSP00000478688.1:p.Ala214Asp
NM_000488.3:c.1256C>A , LRG_577t1:c.1256C>A NP_000479.1:p.Ala419Asp
XM_005245198.2:c.1112C>A XP_005245255.1:p.Ala371Asp
NM_001365052.1:c.1112C>A NP_001351981.1:p.Ala371Asp
NM_000488.4:c.1256C>A MANE Select NP_000479.1:p.Ala419Asp
NM_001365052.2:c.1112C>A NP_001351981.1:p.Ala371Asp
NM_001386302.1:c.1379C>A NP_001373231.1:p.Ala460Asp
NM_001386303.1:c.1337C>A NP_001373232.1:p.Ala446Asp
NM_001386304.1:c.1235C>A NP_001373233.1:p.Ala412Asp
NM_001386305.1:c.1199C>A NP_001373234.1:p.Ala400Asp
NM_001386306.1:c.1040C>A NP_001373235.1:p.Ala347Asp
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