Canonical Allele Identifier: CA343772097
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1657366753

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1367G>A MANE Select ENSP00000356671.3:p.Gly456Asp
ENST00000367698.3:c.1367G>A ENSP00000356671.3:p.Gly456Asp
ENST00000617423.4:c.752G>A ENSP00000478688.1:p.Gly251Asp
NM_000488.3:c.1367G>A , LRG_577t1:c.1367G>A NP_000479.1:p.Gly456Asp
XM_005245198.2:c.1223G>A XP_005245255.1:p.Gly408Asp
NM_001365052.1:c.1223G>A NP_001351981.1:p.Gly408Asp
NM_000488.4:c.1367G>A MANE Select NP_000479.1:p.Gly456Asp
NM_001365052.2:c.1223G>A NP_001351981.1:p.Gly408Asp
NM_001386302.1:c.1490G>A NP_001373231.1:p.Gly497Asp
NM_001386303.1:c.1448G>A NP_001373232.1:p.Gly483Asp
NM_001386304.1:c.1346G>A NP_001373233.1:p.Gly449Asp
NM_001386305.1:c.1310G>A NP_001373234.1:p.Gly437Asp
NM_001386306.1:c.1151G>A NP_001373235.1:p.Gly384Asp