Canonical Allele Identifier: CA1143713195
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909835G= , CM000663.2:g.173909835G= GRCh38
NC_000001.10:g.173878973G= , CM000663.1:g.173878973G= GRCh37
NC_000001.9:g.172145596G= NCBI36
NG_012462.1:g.12544C= , LRG_577:g.12544C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.870C= MANE Select ENSP00000356671.3:p.Phe290=
ENST00000367698.3:c.870C= ENSP00000356671.3:p.Phe290=
ENST00000487183.1:n.521C=
ENST00000617423.4:c.559+2029C= ENSP00000478688.1:n.559+2029C=
NM_000488.3:c.870C= , LRG_577t1:c.870C= NP_000479.1:p.Phe290=
XM_005245198.2:c.726C= XP_005245255.1:p.Phe242=
NM_001365052.1:c.726C= NP_001351981.1:p.Phe242=
NM_000488.4:c.870C= MANE Select NP_000479.1:p.Phe290=
NM_001365052.2:c.726C= NP_001351981.1:p.Phe242=
NM_001386302.1:c.993C= NP_001373231.1:p.Phe331=
NM_001386303.1:c.951C= NP_001373232.1:p.Phe317=
NM_001386304.1:c.849C= NP_001373233.1:p.Phe283=
NM_001386305.1:c.813C= NP_001373234.1:p.Phe271=
NM_001386306.1:c.654C= NP_001373235.1:p.Phe218=