Canonical Allele Identifier: CA421942781
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878700G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909562G>C , CM000663.2:g.173909562G>C GRCh38
NC_000001.10:g.173878700G>C , CM000663.1:g.173878700G>C GRCh37
NC_000001.9:g.172145323G>C NCBI36
NG_012462.1:g.12817C>G , LRG_577:g.12817C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1143C>G MANE Select ENSP00000356671.3:p.Ser381=
ENST00000367698.3:c.1143C>G ENSP00000356671.3:p.Ser381=
ENST00000617423.4:c.560-2069C>G ENSP00000478688.1:n.560-2069C>G
NM_000488.3:c.1143C>G , LRG_577t1:c.1143C>G NP_000479.1:p.Ser381=
XM_005245198.2:c.999C>G XP_005245255.1:p.Ser333=
NM_001365052.1:c.999C>G NP_001351981.1:p.Ser333=
NM_000488.4:c.1143C>G MANE Select NP_000479.1:p.Ser381=
NM_001365052.2:c.999C>G NP_001351981.1:p.Ser333=
NM_001386302.1:c.1266C>G NP_001373231.1:p.Ser422=
NM_001386303.1:c.1224C>G NP_001373232.1:p.Ser408=
NM_001386304.1:c.1122C>G NP_001373233.1:p.Ser374=
NM_001386305.1:c.1086C>G NP_001373234.1:p.Ser362=
NM_001386306.1:c.927C>G NP_001373235.1:p.Ser309=
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