Canonical Allele Identifier: CA1139953648
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904220C= , CM000663.2:g.173904220C= GRCh38
NC_000001.10:g.173873358C= , CM000663.1:g.173873358C= GRCh37
NC_000001.9:g.172139981C= NCBI36
NG_012462.1:g.18159G= , LRG_577:g.18159G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1219-155G= MANE Select ENSP00000356671.3:n.1219-155G=
ENST00000367698.3:c.1219-155G= ENSP00000356671.3:n.1219-155G=
ENST00000617423.4:c.604-155G= ENSP00000478688.1:n.604-155G=
NM_000488.3:c.1219-155G= , LRG_577t1:c.1219-155G= NP_000479.1:n.1219-155G=
XM_005245198.2:c.1075-155G= XP_005245255.1:n.1075-155G=
NM_001365052.1:c.1075-155G= NP_001351981.1:n.1075-155G=
NM_000488.4:c.1219-155G= MANE Select NP_000479.1:n.1219-155G=
NM_001365052.2:c.1075-155G= NP_001351981.1:n.1075-155G=
NM_001386302.1:c.1342-155G= NP_001373231.1:n.1342-155G=
NM_001386303.1:c.1300-155G= NP_001373232.1:n.1300-155G=
NM_001386304.1:c.1198-155G= NP_001373233.1:n.1198-155G=
NM_001386305.1:c.1162-155G= NP_001373234.1:n.1162-155G=
NM_001386306.1:c.1003-155G= NP_001373235.1:n.1003-155G=