Canonical Allele Identifier: CA343772606
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873155C>G (hg19) chr1:g.173904017C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904017C>G , CM000663.2:g.173904017C>G GRCh38
NC_000001.10:g.173873155C>G , CM000663.1:g.173873155C>G GRCh37
NC_000001.9:g.172139778C>G NCBI36
NG_012462.1:g.18362G>C , LRG_577:g.18362G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1267G>C MANE Select ENSP00000356671.3:p.Ala423Pro
ENST00000367698.3:c.1267G>C ENSP00000356671.3:p.Ala423Pro
ENST00000617423.4:c.652G>C ENSP00000478688.1:p.Ala218Pro
NM_000488.3:c.1267G>C , LRG_577t1:c.1267G>C NP_000479.1:p.Ala423Pro
XM_005245198.2:c.1123G>C XP_005245255.1:p.Ala375Pro
NM_001365052.1:c.1123G>C NP_001351981.1:p.Ala375Pro
NM_000488.4:c.1267G>C MANE Select NP_000479.1:p.Ala423Pro
NM_001365052.2:c.1123G>C NP_001351981.1:p.Ala375Pro
NM_001386302.1:c.1390G>C NP_001373231.1:p.Ala464Pro
NM_001386303.1:c.1348G>C NP_001373232.1:p.Ala450Pro
NM_001386304.1:c.1246G>C NP_001373233.1:p.Ala416Pro
NM_001386305.1:c.1210G>C NP_001373234.1:p.Ala404Pro
NM_001386306.1:c.1051G>C NP_001373235.1:p.Ala351Pro
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