Canonical Allele Identifier: CA211882
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161390
ClinVar RCV Id: RCV001099621
dbSNP Id: rs372820797

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909819C>G , CM000663.2:g.173909819C>G GRCh38
NC_000001.10:g.173878957C>G , CM000663.1:g.173878957C>G GRCh37
NC_000001.9:g.172145580C>G NCBI36
NG_012462.1:g.12560G>C , LRG_577:g.12560G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.886G>C MANE Select ENSP00000356671.3:p.Ala296Pro
ENST00000367698.3:c.886G>C ENSP00000356671.3:p.Ala296Pro
ENST00000487183.1:n.537G>C
ENST00000617423.4:c.559+2045G>C ENSP00000478688.1:n.559+2045G>C
NM_000488.3:c.886G>C , LRG_577t1:c.886G>C NP_000479.1:p.Ala296Pro
XM_005245198.2:c.742G>C XP_005245255.1:p.Ala248Pro
NM_001365052.1:c.742G>C NP_001351981.1:p.Ala248Pro
NM_000488.4:c.886G>C MANE Select NP_000479.1:p.Ala296Pro
NM_001365052.2:c.742G>C NP_001351981.1:p.Ala248Pro
NM_001386302.1:c.1009G>C NP_001373231.1:p.Ala337Pro
NM_001386303.1:c.967G>C NP_001373232.1:p.Ala323Pro
NM_001386304.1:c.865G>C NP_001373233.1:p.Ala289Pro
NM_001386305.1:c.829G>C NP_001373234.1:p.Ala277Pro
NM_001386306.1:c.670G>C NP_001373235.1:p.Ala224Pro