Canonical Allele Identifier: CA343772391
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2734037
ClinVar RCV Id: RCV003527184
dbSNP Id: rs1301351856

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903973G>C , CM000663.2:g.173903973G>C GRCh38
NC_000001.10:g.173873111G>C , CM000663.1:g.173873111G>C GRCh37
NC_000001.9:g.172139734G>C NCBI36
NG_012462.1:g.18406C>G , LRG_577:g.18406C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1311C>G MANE Select ENSP00000356671.3:p.Asn437Lys
ENST00000367698.3:c.1311C>G ENSP00000356671.3:p.Asn437Lys
ENST00000617423.4:c.696C>G ENSP00000478688.1:p.Asn232Lys
NM_000488.3:c.1311C>G , LRG_577t1:c.1311C>G NP_000479.1:p.Asn437Lys
XM_005245198.2:c.1167C>G XP_005245255.1:p.Asn389Lys
NM_001365052.1:c.1167C>G NP_001351981.1:p.Asn389Lys
NM_000488.4:c.1311C>G MANE Select NP_000479.1:p.Asn437Lys
NM_001365052.2:c.1167C>G NP_001351981.1:p.Asn389Lys
NM_001386302.1:c.1434C>G NP_001373231.1:p.Asn478Lys
NM_001386303.1:c.1392C>G NP_001373232.1:p.Asn464Lys
NM_001386304.1:c.1290C>G NP_001373233.1:p.Asn430Lys
NM_001386305.1:c.1254C>G NP_001373234.1:p.Asn418Lys
NM_001386306.1:c.1095C>G NP_001373235.1:p.Asn365Lys