Canonical Allele Identifier: CA1207937044
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909910G= , CM000663.2:g.173909910G= GRCh38
NC_000001.10:g.173879048G= , CM000663.1:g.173879048G= GRCh37
NC_000001.9:g.172145671G= NCBI36
NG_012462.1:g.12469C= , LRG_577:g.12469C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.795C= MANE Select ENSP00000356671.3:p.Asn265=
ENST00000367698.3:c.795C= ENSP00000356671.3:p.Asn265=
ENST00000487183.1:n.446C=
ENST00000617423.4:c.559+1954C= ENSP00000478688.1:n.559+1954C=
NM_000488.3:c.795C= , LRG_577t1:c.795C= NP_000479.1:p.Asn265=
XM_005245198.2:c.651C= XP_005245255.1:p.Asn217=
NM_001365052.1:c.651C= NP_001351981.1:p.Asn217=
NM_000488.4:c.795C= MANE Select NP_000479.1:p.Asn265=
NM_001365052.2:c.651C= NP_001351981.1:p.Asn217=
NM_001386302.1:c.918C= NP_001373231.1:p.Asn306=
NM_001386303.1:c.876C= NP_001373232.1:p.Asn292=
NM_001386304.1:c.774C= NP_001373233.1:p.Asn258=
NM_001386305.1:c.763-25C= NP_001373234.1:n.763-25C=
NM_001386306.1:c.579C= NP_001373235.1:p.Asn193=