Canonical Allele Identifier: CA421942983
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878880C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909742C>T , CM000663.2:g.173909742C>T GRCh38
NC_000001.10:g.173878880C>T , CM000663.1:g.173878880C>T GRCh37
NC_000001.9:g.172145503C>T NCBI36
NG_012462.1:g.12637G>A , LRG_577:g.12637G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.963G>A MANE Select ENSP00000356671.3:p.Glu321=
ENST00000367698.3:c.963G>A ENSP00000356671.3:p.Glu321=
ENST00000487183.1:n.614G>A
ENST00000617423.4:c.559+2122G>A ENSP00000478688.1:n.559+2122G>A
NM_000488.3:c.963G>A , LRG_577t1:c.963G>A NP_000479.1:p.Glu321=
XM_005245198.2:c.819G>A XP_005245255.1:p.Glu273=
NM_001365052.1:c.819G>A NP_001351981.1:p.Glu273=
NM_000488.4:c.963G>A MANE Select NP_000479.1:p.Glu321=
NM_001365052.2:c.819G>A NP_001351981.1:p.Glu273=
NM_001386302.1:c.1086G>A NP_001373231.1:p.Glu362=
NM_001386303.1:c.1044G>A NP_001373232.1:p.Glu348=
NM_001386304.1:c.942G>A NP_001373233.1:p.Glu314=
NM_001386305.1:c.906G>A NP_001373234.1:p.Glu302=
NM_001386306.1:c.747G>A NP_001373235.1:p.Glu249=