Canonical Allele Identifier: CA1141581220
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173910849A= , CM000663.2:g.173910849A= GRCh38
NC_000001.10:g.173879987A= , CM000663.1:g.173879987A= GRCh37
NC_000001.9:g.172146610A= NCBI36
NG_012462.1:g.11530T= , LRG_577:g.11530T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.667T= MANE Select ENSP00000356671.3:p.Ser223=
ENST00000367698.3:c.667T= ENSP00000356671.3:p.Ser223=
ENST00000487183.1:n.330-12T=
ENST00000617423.4:c.559+1015T= ENSP00000478688.1:n.559+1015T=
NM_000488.3:c.667T= , LRG_577t1:c.667T= NP_000479.1:p.Ser223=
XM_005245198.2:c.523T= XP_005245255.1:p.Ser175=
NM_001365052.1:c.523T= NP_001351981.1:p.Ser175=
NM_000488.4:c.667T= MANE Select NP_000479.1:p.Ser223=
NM_001365052.2:c.523T= NP_001351981.1:p.Ser175=
NM_001386302.1:c.667T= NP_001373231.1:p.Ser223=
NM_001386303.1:c.748T= NP_001373232.1:p.Ser250=
NM_001386304.1:c.667T= NP_001373233.1:p.Ser223=
NM_001386305.1:c.667T= NP_001373234.1:p.Ser223=
NM_001386306.1:c.451T= NP_001373235.1:p.Ser151=