Canonical Allele Identifier: CA343773947
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878849T>G (hg19) chr1:g.173909711T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909711T>G , CM000663.2:g.173909711T>G GRCh38
NC_000001.10:g.173878849T>G , CM000663.1:g.173878849T>G GRCh37
NC_000001.9:g.172145472T>G NCBI36
NG_012462.1:g.12668A>C , LRG_577:g.12668A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.994A>C MANE Select ENSP00000356671.3:p.Thr332Pro
ENST00000367698.3:c.994A>C ENSP00000356671.3:p.Thr332Pro
ENST00000617423.4:c.559+2153A>C ENSP00000478688.1:n.559+2153A>C
NM_000488.3:c.994A>C , LRG_577t1:c.994A>C NP_000479.1:p.Thr332Pro
XM_005245198.2:c.850A>C XP_005245255.1:p.Thr284Pro
NM_001365052.1:c.850A>C NP_001351981.1:p.Thr284Pro
NM_000488.4:c.994A>C MANE Select NP_000479.1:p.Thr332Pro
NM_001365052.2:c.850A>C NP_001351981.1:p.Thr284Pro
NM_001386302.1:c.1117A>C NP_001373231.1:p.Thr373Pro
NM_001386303.1:c.1075A>C NP_001373232.1:p.Thr359Pro
NM_001386304.1:c.973A>C NP_001373233.1:p.Thr325Pro
NM_001386305.1:c.937A>C NP_001373234.1:p.Thr313Pro
NM_001386306.1:c.778A>C NP_001373235.1:p.Thr260Pro
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