Canonical Allele Identifier: CA1148869223
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903914C= , CM000663.2:g.173903914C= GRCh38
NC_000001.10:g.173873052C= , CM000663.1:g.173873052C= GRCh37
NC_000001.9:g.172139675C= NCBI36
NG_012462.1:g.18465G= , LRG_577:g.18465G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1370G= MANE Select ENSP00000356671.3:p.Arg457=
ENST00000367698.3:c.1370G= ENSP00000356671.3:p.Arg457=
ENST00000617423.4:c.755G= ENSP00000478688.1:p.Arg252=
NM_000488.3:c.1370G= , LRG_577t1:c.1370G= NP_000479.1:p.Arg457=
XM_005245198.2:c.1226G= XP_005245255.1:p.Arg409=
NM_001365052.1:c.1226G= NP_001351981.1:p.Arg409=
NM_000488.4:c.1370G= MANE Select NP_000479.1:p.Arg457=
NM_001365052.2:c.1226G= NP_001351981.1:p.Arg409=
NM_001386302.1:c.1493G= NP_001373231.1:p.Arg498=
NM_001386303.1:c.1451G= NP_001373232.1:p.Arg484=
NM_001386304.1:c.1349G= NP_001373233.1:p.Arg450=
NM_001386305.1:c.1313G= NP_001373234.1:p.Arg438=
NM_001386306.1:c.1154G= NP_001373235.1:p.Arg385=