Canonical Allele Identifier: CA1207937062
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909974C= , CM000663.2:g.173909974C= GRCh38
NC_000001.10:g.173879112C= , CM000663.1:g.173879112C= GRCh37
NC_000001.9:g.172145735C= NCBI36
NG_012462.1:g.12405G= , LRG_577:g.12405G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763-32G= MANE Select ENSP00000356671.3:n.763-32G=
ENST00000367698.3:c.763-32G= ENSP00000356671.3:n.763-32G=
ENST00000487183.1:n.414-32G=
ENST00000617423.4:c.559+1890G= ENSP00000478688.1:n.559+1890G=
NM_000488.3:c.763-32G= , LRG_577t1:c.763-32G= NP_000479.1:n.763-32G=
XM_005245198.2:c.619-32G= XP_005245255.1:n.619-32G=
NM_001365052.1:c.619-32G= NP_001351981.1:n.619-32G=
NM_000488.4:c.763-32G= MANE Select NP_000479.1:n.763-32G=
NM_001365052.2:c.619-32G= NP_001351981.1:n.619-32G=
NM_001386302.1:c.886-32G= NP_001373231.1:n.886-32G=
NM_001386303.1:c.844-32G= NP_001373232.1:n.844-32G=
NM_001386304.1:c.742-32G= NP_001373233.1:n.742-32G=
NM_001386305.1:c.763-89G= NP_001373234.1:n.763-89G=
NM_001386306.1:c.547-32G= NP_001373235.1:n.547-32G=