Canonical Allele Identifier: CA2580060354
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173914874_173914875delinsAG , CM000663.2:g.173914874_173914875delinsAG GRCh38
NC_000001.10:g.173884012_173884013delinsAG , CM000663.1:g.173884012_173884013delinsAG GRCh37
NC_000001.9:g.172150635_172150636delinsAG NCBI36
NG_012462.1:g.7504_7505delinsCT , LRG_577:g.7504_7505delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.86_87delinsCT MANE Select ENSP00000356671.3:p.Cys29Ser
ENST00000367698.3:c.86_87delinsCT ENSP00000356671.3:p.Cys29Ser
ENST00000494024.1:n.312_313delinsCT
ENST00000617423.4:c.86_87delinsCT ENSP00000478688.1:p.Cys29Ser
NM_000488.3:c.86_87delinsCT , LRG_577t1:c.86_87delinsCT NP_000479.1:p.Cys29Ser
XM_005245198.2:c.-59_-58delinsCT XP_005245255.1:n.-59_-58delinsCT
NM_001365052.1:c.-59_-58delinsCT NP_001351981.1:n.-59_-58delinsCT
NM_000488.4:c.86_87delinsCT MANE Select NP_000479.1:p.Cys29Ser
NM_001365052.2:c.-59_-58delinsCT NP_001351981.1:n.-59_-58delinsCT
NM_001386302.1:c.86_87delinsCT NP_001373231.1:p.Cys29Ser
NM_001386303.1:c.167_168delinsCT NP_001373232.1:p.Cys56Ser
NM_001386304.1:c.86_87delinsCT NP_001373233.1:p.Cys29Ser
NM_001386305.1:c.86_87delinsCT NP_001373234.1:p.Cys29Ser
NM_001386306.1:c.86_87delinsCT NP_001373235.1:p.Cys29Ser