Canonical Allele Identifier: CA1144147984
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909639G= , CM000663.2:g.173909639G= GRCh38
NC_000001.10:g.173878777G= , CM000663.1:g.173878777G= GRCh37
NC_000001.9:g.172145400G= NCBI36
NG_012462.1:g.12740C= , LRG_577:g.12740C=

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1066C= MANE Select ENSP00000356671.3:p.Arg356=
ENST00000367698.3:c.1066C= ENSP00000356671.3:p.Arg356=
ENST00000617423.4:c.560-2146C= ENSP00000478688.1:n.560-2146C=
NM_000488.3:c.1066C= , LRG_577t1:c.1066C= NP_000479.1:p.Arg356=
XM_005245198.2:c.922C= XP_005245255.1:p.Arg308=
NM_001365052.1:c.922C= NP_001351981.1:p.Arg308=
NM_000488.4:c.1066C= MANE Select NP_000479.1:p.Arg356=
NM_001365052.2:c.922C= NP_001351981.1:p.Arg308=
NM_001386302.1:c.1189C= NP_001373231.1:p.Arg397=
NM_001386303.1:c.1147C= NP_001373232.1:p.Arg383=
NM_001386304.1:c.1045C= NP_001373233.1:p.Arg349=
NM_001386305.1:c.1009C= NP_001373234.1:p.Arg337=
NM_001386306.1:c.850C= NP_001373235.1:p.Arg284=