Canonical Allele Identifier: CA1207937043
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909908G= , CM000663.2:g.173909908G= GRCh38
NC_000001.10:g.173879046G= , CM000663.1:g.173879046G= GRCh37
NC_000001.9:g.172145669G= NCBI36
NG_012462.1:g.12471C= , LRG_577:g.12471C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.797C= MANE Select ENSP00000356671.3:p.Thr266=
ENST00000367698.3:c.797C= ENSP00000356671.3:p.Thr266=
ENST00000487183.1:n.448C=
ENST00000617423.4:c.559+1956C= ENSP00000478688.1:n.559+1956C=
NM_000488.3:c.797C= , LRG_577t1:c.797C= NP_000479.1:p.Thr266=
XM_005245198.2:c.653C= XP_005245255.1:p.Thr218=
NM_001365052.1:c.653C= NP_001351981.1:p.Thr218=
NM_000488.4:c.797C= MANE Select NP_000479.1:p.Thr266=
NM_001365052.2:c.653C= NP_001351981.1:p.Thr218=
NM_001386302.1:c.920C= NP_001373231.1:p.Thr307=
NM_001386303.1:c.878C= NP_001373232.1:p.Thr293=
NM_001386304.1:c.776C= NP_001373233.1:p.Thr259=
NM_001386305.1:c.763-23C= NP_001373234.1:n.763-23C=
NM_001386306.1:c.581C= NP_001373235.1:p.Thr194=