Canonical Allele Identifier: CA343773633
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909630C>A , CM000663.2:g.173909630C>A GRCh38
NC_000001.10:g.173878768C>A , CM000663.1:g.173878768C>A GRCh37
NC_000001.9:g.172145391C>A NCBI36
NG_012462.1:g.12749G>T , LRG_577:g.12749G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1075G>T MANE Select ENSP00000356671.3:p.Asp359Tyr
ENST00000367698.3:c.1075G>T ENSP00000356671.3:p.Asp359Tyr
ENST00000617423.4:c.560-2137G>T ENSP00000478688.1:n.560-2137G>T
NM_000488.3:c.1075G>T , LRG_577t1:c.1075G>T NP_000479.1:p.Asp359Tyr
XM_005245198.2:c.931G>T XP_005245255.1:p.Asp311Tyr
NM_001365052.1:c.931G>T NP_001351981.1:p.Asp311Tyr
NM_000488.4:c.1075G>T MANE Select NP_000479.1:p.Asp359Tyr
NM_001365052.2:c.931G>T NP_001351981.1:p.Asp311Tyr
NM_001386302.1:c.1198G>T NP_001373231.1:p.Asp400Tyr
NM_001386303.1:c.1156G>T NP_001373232.1:p.Asp386Tyr
NM_001386304.1:c.1054G>T NP_001373233.1:p.Asp352Tyr
NM_001386305.1:c.1018G>T NP_001373234.1:p.Asp340Tyr
NM_001386306.1:c.859G>T NP_001373235.1:p.Asp287Tyr