Canonical Allele Identifier: CA343772477
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873125T>G (hg19) chr1:g.173903987T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903987T>G , CM000663.2:g.173903987T>G GRCh38
NC_000001.10:g.173873125T>G , CM000663.1:g.173873125T>G GRCh37
NC_000001.9:g.172139748T>G NCBI36
NG_012462.1:g.18392A>C , LRG_577:g.18392A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1297A>C MANE Select ENSP00000356671.3:p.Thr433Pro
ENST00000367698.3:c.1297A>C ENSP00000356671.3:p.Thr433Pro
ENST00000617423.4:c.682A>C ENSP00000478688.1:p.Thr228Pro
NM_000488.3:c.1297A>C , LRG_577t1:c.1297A>C NP_000479.1:p.Thr433Pro
XM_005245198.2:c.1153A>C XP_005245255.1:p.Thr385Pro
NM_001365052.1:c.1153A>C NP_001351981.1:p.Thr385Pro
NM_000488.4:c.1297A>C MANE Select NP_000479.1:p.Thr433Pro
NM_001365052.2:c.1153A>C NP_001351981.1:p.Thr385Pro
NM_001386302.1:c.1420A>C NP_001373231.1:p.Thr474Pro
NM_001386303.1:c.1378A>C NP_001373232.1:p.Thr460Pro
NM_001386304.1:c.1276A>C NP_001373233.1:p.Thr426Pro
NM_001386305.1:c.1240A>C NP_001373234.1:p.Thr414Pro
NM_001386306.1:c.1081A>C NP_001373235.1:p.Thr361Pro
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