Canonical Allele Identifier: CA1207936849
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909434A= , CM000663.2:g.173909434A= GRCh38
NC_000001.10:g.173878572A= , CM000663.1:g.173878572A= GRCh37
NC_000001.9:g.172145195A= NCBI36
NG_012462.1:g.12945T= , LRG_577:g.12945T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1153+118T= MANE Select ENSP00000356671.3:n.1153+118T=
ENST00000367698.3:c.1153+118T= ENSP00000356671.3:n.1153+118T=
ENST00000617423.4:c.560-1941T= ENSP00000478688.1:n.560-1941T=
NM_000488.3:c.1153+118T= , LRG_577t1:c.1153+118T= NP_000479.1:n.1153+118T=
XM_005245198.2:c.1009+118T= XP_005245255.1:n.1009+118T=
NM_001365052.1:c.1009+118T= NP_001351981.1:n.1009+118T=
NM_000488.4:c.1153+118T= MANE Select NP_000479.1:n.1153+118T=
NM_001365052.2:c.1009+118T= NP_001351981.1:n.1009+118T=
NM_001386302.1:c.1276+118T= NP_001373231.1:n.1276+118T=
NM_001386303.1:c.1234+118T= NP_001373232.1:n.1234+118T=
NM_001386304.1:c.1132+118T= NP_001373233.1:n.1132+118T=
NM_001386305.1:c.1096+118T= NP_001373234.1:n.1096+118T=
NM_001386306.1:c.937+118T= NP_001373235.1:n.937+118T=