Canonical Allele Identifier: CA1207936897
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909565C= , CM000663.2:g.173909565C= GRCh38
NC_000001.10:g.173878703C= , CM000663.1:g.173878703C= GRCh37
NC_000001.9:g.172145326C= NCBI36
NG_012462.1:g.12814G= , LRG_577:g.12814G=

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1140G= MANE Select ENSP00000356671.3:p.Lys380=
ENST00000367698.3:c.1140G= ENSP00000356671.3:p.Lys380=
ENST00000617423.4:c.560-2072G= ENSP00000478688.1:n.560-2072G=
NM_000488.3:c.1140G= , LRG_577t1:c.1140G= NP_000479.1:p.Lys380=
XM_005245198.2:c.996G= XP_005245255.1:p.Lys332=
NM_001365052.1:c.996G= NP_001351981.1:p.Lys332=
NM_000488.4:c.1140G= MANE Select NP_000479.1:p.Lys380=
NM_001365052.2:c.996G= NP_001351981.1:p.Lys332=
NM_001386302.1:c.1263G= NP_001373231.1:p.Lys421=
NM_001386303.1:c.1221G= NP_001373232.1:p.Lys407=
NM_001386304.1:c.1119G= NP_001373233.1:p.Lys373=
NM_001386305.1:c.1083G= NP_001373234.1:p.Lys361=
NM_001386306.1:c.924G= NP_001373235.1:p.Lys308=