Canonical Allele Identifier: CA1207934374
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903963G= , CM000663.2:g.173903963G= GRCh38
NC_000001.10:g.173873101G= , CM000663.1:g.173873101G= GRCh37
NC_000001.9:g.172139724G= NCBI36
NG_012462.1:g.18416C= , LRG_577:g.18416C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1321C= MANE Select ENSP00000356671.3:p.Leu441=
ENST00000367698.3:c.1321C= ENSP00000356671.3:p.Leu441=
ENST00000617423.4:c.706C= ENSP00000478688.1:p.Leu236=
NM_000488.3:c.1321C= , LRG_577t1:c.1321C= NP_000479.1:p.Leu441=
XM_005245198.2:c.1177C= XP_005245255.1:p.Leu393=
NM_001365052.1:c.1177C= NP_001351981.1:p.Leu393=
NM_000488.4:c.1321C= MANE Select NP_000479.1:p.Leu441=
NM_001365052.2:c.1177C= NP_001351981.1:p.Leu393=
NM_001386302.1:c.1444C= NP_001373231.1:p.Leu482=
NM_001386303.1:c.1402C= NP_001373232.1:p.Leu468=
NM_001386304.1:c.1300C= NP_001373233.1:p.Leu434=
NM_001386305.1:c.1264C= NP_001373234.1:p.Leu422=
NM_001386306.1:c.1105C= NP_001373235.1:p.Leu369=