Canonical Allele Identifier: CA1207934363
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903917C= , CM000663.2:g.173903917C= GRCh38
NC_000001.10:g.173873055C= , CM000663.1:g.173873055C= GRCh37
NC_000001.9:g.172139678C= NCBI36
NG_012462.1:g.18462G= , LRG_577:g.18462G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1367G= MANE Select ENSP00000356671.3:p.Gly456=
ENST00000367698.3:c.1367G= ENSP00000356671.3:p.Gly456=
ENST00000617423.4:c.752G= ENSP00000478688.1:p.Gly251=
NM_000488.3:c.1367G= , LRG_577t1:c.1367G= NP_000479.1:p.Gly456=
XM_005245198.2:c.1223G= XP_005245255.1:p.Gly408=
NM_001365052.1:c.1223G= NP_001351981.1:p.Gly408=
NM_000488.4:c.1367G= MANE Select NP_000479.1:p.Gly456=
NM_001365052.2:c.1223G= NP_001351981.1:p.Gly408=
NM_001386302.1:c.1490G= NP_001373231.1:p.Gly497=
NM_001386303.1:c.1448G= NP_001373232.1:p.Gly483=
NM_001386304.1:c.1346G= NP_001373233.1:p.Gly449=
NM_001386305.1:c.1310G= NP_001373234.1:p.Gly437=
NM_001386306.1:c.1151G= NP_001373235.1:p.Gly384=