Canonical Allele Identifier: CA1207937623
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173911326G= , CM000663.2:g.173911326G= GRCh38
NC_000001.10:g.173880464G= , CM000663.1:g.173880464G= GRCh37
NC_000001.9:g.172147087G= NCBI36
NG_012462.1:g.11053C= , LRG_577:g.11053C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.625-435C= MANE Select ENSP00000356671.3:n.625-435C=
ENST00000367698.3:c.625-435C= ENSP00000356671.3:n.625-435C=
ENST00000487183.1:n.329+473C=
ENST00000617423.4:c.559+538C= ENSP00000478688.1:n.559+538C=
NM_000488.3:c.625-435C= , LRG_577t1:c.625-435C= NP_000479.1:n.625-435C=
XM_005245198.2:c.481-435C= XP_005245255.1:n.481-435C=
NM_001365052.1:c.481-435C= NP_001351981.1:n.481-435C=
NM_000488.4:c.625-435C= MANE Select NP_000479.1:n.625-435C=
NM_001365052.2:c.481-435C= NP_001351981.1:n.481-435C=
NM_001386302.1:c.625-435C= NP_001373231.1:n.625-435C=
NM_001386303.1:c.706-435C= NP_001373232.1:n.706-435C=
NM_001386304.1:c.625-435C= NP_001373233.1:n.625-435C=
NM_001386305.1:c.625-435C= NP_001373234.1:n.625-435C=
NM_001386306.1:c.409-435C= NP_001373235.1:n.409-435C=