Canonical Allele Identifier: CA1207936366
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173908391G= , CM000663.2:g.173908391G= GRCh38
NC_000001.10:g.173877529G= , CM000663.1:g.173877529G= GRCh37
NC_000001.9:g.172144152G= NCBI36
NG_012462.1:g.13988C= , LRG_577:g.13988C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1154-877C= MANE Select ENSP00000356671.3:n.1154-877C=
ENST00000367698.3:c.1154-877C= ENSP00000356671.3:n.1154-877C=
ENST00000617423.4:c.560-898C= ENSP00000478688.1:n.560-898C=
NM_000488.3:c.1154-877C= , LRG_577t1:c.1154-877C= NP_000479.1:n.1154-877C=
XM_005245198.2:c.1010-877C= XP_005245255.1:n.1010-877C=
NM_001365052.1:c.1010-877C= NP_001351981.1:n.1010-877C=
NM_000488.4:c.1154-877C= MANE Select NP_000479.1:n.1154-877C=
NM_001365052.2:c.1010-877C= NP_001351981.1:n.1010-877C=
NM_001386302.1:c.1277-877C= NP_001373231.1:n.1277-877C=
NM_001386303.1:c.1235-877C= NP_001373232.1:n.1235-877C=
NM_001386304.1:c.1133-877C= NP_001373233.1:n.1133-877C=
NM_001386305.1:c.1097-877C= NP_001373234.1:n.1097-877C=
NM_001386306.1:c.938-877C= NP_001373235.1:n.938-877C=