Canonical Allele Identifier: CA1207937048
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909931C= , CM000663.2:g.173909931C= GRCh38
NC_000001.10:g.173879069C= , CM000663.1:g.173879069C= GRCh37
NC_000001.9:g.172145692C= NCBI36
NG_012462.1:g.12448G= , LRG_577:g.12448G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.774G= MANE Select ENSP00000356671.3:p.Lys258=
ENST00000367698.3:c.774G= ENSP00000356671.3:p.Lys258=
ENST00000487183.1:n.425G=
ENST00000617423.4:c.559+1933G= ENSP00000478688.1:n.559+1933G=
NM_000488.3:c.774G= , LRG_577t1:c.774G= NP_000479.1:p.Lys258=
XM_005245198.2:c.630G= XP_005245255.1:p.Lys210=
NM_001365052.1:c.630G= NP_001351981.1:p.Lys210=
NM_000488.4:c.774G= MANE Select NP_000479.1:p.Lys258=
NM_001365052.2:c.630G= NP_001351981.1:p.Lys210=
NM_001386302.1:c.897G= NP_001373231.1:p.Lys299=
NM_001386303.1:c.855G= NP_001373232.1:p.Lys285=
NM_001386304.1:c.753G= NP_001373233.1:p.Lys251=
NM_001386305.1:c.763-46G= NP_001373234.1:n.763-46G=
NM_001386306.1:c.558G= NP_001373235.1:p.Lys186=