Canonical Allele Identifier: CA210783
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 18032
ClinVar RCV Id: RCV000019648
dbSNP Id: rs121909565

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909564A>G , CM000663.2:g.173909564A>G GRCh38
NC_000001.10:g.173878702A>G , CM000663.1:g.173878702A>G GRCh37
NC_000001.9:g.172145325A>G NCBI36
NG_012462.1:g.12815T>C , LRG_577:g.12815T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1141T>C MANE Select ENSP00000356671.3:p.Ser381Pro
ENST00000367698.3:c.1141T>C ENSP00000356671.3:p.Ser381Pro
ENST00000617423.4:c.560-2071T>C ENSP00000478688.1:n.560-2071T>C
NM_000488.3:c.1141T>C , LRG_577t1:c.1141T>C NP_000479.1:p.Ser381Pro
XM_005245198.2:c.997T>C XP_005245255.1:p.Ser333Pro
NM_001365052.1:c.997T>C NP_001351981.1:p.Ser333Pro
NM_000488.4:c.1141T>C MANE Select NP_000479.1:p.Ser381Pro
NM_001365052.2:c.997T>C NP_001351981.1:p.Ser333Pro
NM_001386302.1:c.1264T>C NP_001373231.1:p.Ser422Pro
NM_001386303.1:c.1222T>C NP_001373232.1:p.Ser408Pro
NM_001386304.1:c.1120T>C NP_001373233.1:p.Ser374Pro
NM_001386305.1:c.1084T>C NP_001373234.1:p.Ser362Pro
NM_001386306.1:c.925T>C NP_001373235.1:p.Ser309Pro