Canonical Allele Identifier: CA1207937141
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173910162C= , CM000663.2:g.173910162C= GRCh38
NC_000001.10:g.173879300C= , CM000663.1:g.173879300C= GRCh37
NC_000001.9:g.172145923C= NCBI36
NG_012462.1:g.12217G= , LRG_577:g.12217G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763-220G= MANE Select ENSP00000356671.3:n.763-220G=
ENST00000367698.3:c.763-220G= ENSP00000356671.3:n.763-220G=
ENST00000487183.1:n.414-220G=
ENST00000617423.4:c.559+1702G= ENSP00000478688.1:n.559+1702G=
NM_000488.3:c.763-220G= , LRG_577t1:c.763-220G= NP_000479.1:n.763-220G=
XM_005245198.2:c.619-220G= XP_005245255.1:n.619-220G=
NM_001365052.1:c.619-220G= NP_001351981.1:n.619-220G=
NM_000488.4:c.763-220G= MANE Select NP_000479.1:n.763-220G=
NM_001365052.2:c.619-220G= NP_001351981.1:n.619-220G=
NM_001386302.1:c.886-220G= NP_001373231.1:n.886-220G=
NM_001386303.1:c.844-220G= NP_001373232.1:n.844-220G=
NM_001386304.1:c.742-220G= NP_001373233.1:n.742-220G=
NM_001386305.1:c.763-277G= NP_001373234.1:n.763-277G=
NM_001386306.1:c.547-220G= NP_001373235.1:n.547-220G=