Canonical Allele Identifier: CA343772472
Gene: SERPINC1 HGNC NCBI

Linked Data

COSMIC: COSM1320733
MyVariant Identifiers: chr1:g.173873124G>C (hg19) chr1:g.173903986G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903986G>C , CM000663.2:g.173903986G>C GRCh38
NC_000001.10:g.173873124G>C , CM000663.1:g.173873124G>C GRCh37
NC_000001.9:g.172139747G>C NCBI36
NG_012462.1:g.18393C>G , LRG_577:g.18393C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1298C>G MANE Select ENSP00000356671.3:p.Thr433Ser
ENST00000367698.3:c.1298C>G ENSP00000356671.3:p.Thr433Ser
ENST00000617423.4:c.683C>G ENSP00000478688.1:p.Thr228Ser
NM_000488.3:c.1298C>G , LRG_577t1:c.1298C>G NP_000479.1:p.Thr433Ser
XM_005245198.2:c.1154C>G XP_005245255.1:p.Thr385Ser
NM_001365052.1:c.1154C>G NP_001351981.1:p.Thr385Ser
NM_000488.4:c.1298C>G MANE Select NP_000479.1:p.Thr433Ser
NM_001365052.2:c.1154C>G NP_001351981.1:p.Thr385Ser
NM_001386302.1:c.1421C>G NP_001373231.1:p.Thr474Ser
NM_001386303.1:c.1379C>G NP_001373232.1:p.Thr460Ser
NM_001386304.1:c.1277C>G NP_001373233.1:p.Thr426Ser
NM_001386305.1:c.1241C>G NP_001373234.1:p.Thr414Ser
NM_001386306.1:c.1082C>G NP_001373235.1:p.Thr361Ser
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