Canonical Allele Identifier: CA1207936982
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909753G= , CM000663.2:g.173909753G= GRCh38
NC_000001.10:g.173878891G= , CM000663.1:g.173878891G= GRCh37
NC_000001.9:g.172145514G= NCBI36
NG_012462.1:g.12626C= , LRG_577:g.12626C=

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.952C= MANE Select ENSP00000356671.3:p.Pro318=
ENST00000367698.3:c.952C= ENSP00000356671.3:p.Pro318=
ENST00000487183.1:n.603C=
ENST00000617423.4:c.559+2111C= ENSP00000478688.1:n.559+2111C=
NM_000488.3:c.952C= , LRG_577t1:c.952C= NP_000479.1:p.Pro318=
XM_005245198.2:c.808C= XP_005245255.1:p.Pro270=
NM_001365052.1:c.808C= NP_001351981.1:p.Pro270=
NM_000488.4:c.952C= MANE Select NP_000479.1:p.Pro318=
NM_001365052.2:c.808C= NP_001351981.1:p.Pro270=
NM_001386302.1:c.1075C= NP_001373231.1:p.Pro359=
NM_001386303.1:c.1033C= NP_001373232.1:p.Pro345=
NM_001386304.1:c.931C= NP_001373233.1:p.Pro311=
NM_001386305.1:c.895C= NP_001373234.1:p.Pro299=
NM_001386306.1:c.736C= NP_001373235.1:p.Pro246=