Canonical Allele Identifier: CA343772447
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2202884
ClinVar RCV Id: RCV002648222

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903982G>T , CM000663.2:g.173903982G>T GRCh38
NC_000001.10:g.173873120G>T , CM000663.1:g.173873120G>T GRCh37
NC_000001.9:g.172139743G>T NCBI36
NG_012462.1:g.18397C>A , LRG_577:g.18397C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1302C>A MANE Select ENSP00000356671.3:p.Phe434Leu
ENST00000367698.3:c.1302C>A ENSP00000356671.3:p.Phe434Leu
ENST00000617423.4:c.687C>A ENSP00000478688.1:p.Phe229Leu
NM_000488.3:c.1302C>A , LRG_577t1:c.1302C>A NP_000479.1:p.Phe434Leu
XM_005245198.2:c.1158C>A XP_005245255.1:p.Phe386Leu
NM_001365052.1:c.1158C>A NP_001351981.1:p.Phe386Leu
NM_000488.4:c.1302C>A MANE Select NP_000479.1:p.Phe434Leu
NM_001365052.2:c.1158C>A NP_001351981.1:p.Phe386Leu
NM_001386302.1:c.1425C>A NP_001373231.1:p.Phe475Leu
NM_001386303.1:c.1383C>A NP_001373232.1:p.Phe461Leu
NM_001386304.1:c.1281C>A NP_001373233.1:p.Phe427Leu
NM_001386305.1:c.1245C>A NP_001373234.1:p.Phe415Leu
NM_001386306.1:c.1086C>A NP_001373235.1:p.Phe362Leu