Canonical Allele Identifier: CA343773996
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878861C>A (hg19) chr1:g.173909723C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909723C>A , CM000663.2:g.173909723C>A GRCh38
NC_000001.10:g.173878861C>A , CM000663.1:g.173878861C>A GRCh37
NC_000001.9:g.172145484C>A NCBI36
NG_012462.1:g.12656G>T , LRG_577:g.12656G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.982G>T MANE Select ENSP00000356671.3:p.Glu328Ter
ENST00000367698.3:c.982G>T ENSP00000356671.3:p.Glu328Ter
ENST00000617423.4:c.559+2141G>T ENSP00000478688.1:n.559+2141G>T
NM_000488.3:c.982G>T , LRG_577t1:c.982G>T NP_000479.1:p.Glu328Ter
XM_005245198.2:c.838G>T XP_005245255.1:p.Glu280Ter
NM_001365052.1:c.838G>T NP_001351981.1:p.Glu280Ter
NM_000488.4:c.982G>T MANE Select NP_000479.1:p.Glu328Ter
NM_001365052.2:c.838G>T NP_001351981.1:p.Glu280Ter
NM_001386302.1:c.1105G>T NP_001373231.1:p.Glu369Ter
NM_001386303.1:c.1063G>T NP_001373232.1:p.Glu355Ter
NM_001386304.1:c.961G>T NP_001373233.1:p.Glu321Ter
NM_001386305.1:c.925G>T NP_001373234.1:p.Glu309Ter
NM_001386306.1:c.766G>T NP_001373235.1:p.Glu256Ter
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