Canonical Allele Identifier: CA210756
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 18011
dbSNP Id: rs121909551

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173914743G>A , CM000663.2:g.173914743G>A GRCh38
NC_000001.10:g.173883881G>A , CM000663.1:g.173883881G>A GRCh37
NC_000001.9:g.172150504G>A NCBI36
NG_012462.1:g.7636C>T , LRG_577:g.7636C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.218C>T MANE Select ENSP00000356671.3:p.Pro73Leu
ENST00000367698.3:c.218C>T ENSP00000356671.3:p.Pro73Leu
ENST00000494024.1:n.444C>T
ENST00000617423.4:c.218C>T ENSP00000478688.1:p.Pro73Leu
NM_000488.3:c.218C>T , LRG_577t1:c.218C>T NP_000479.1:p.Pro73Leu
XM_005245198.2:c.74C>T XP_005245255.1:p.Pro25Leu
NM_001365052.1:c.74C>T NP_001351981.1:p.Pro25Leu
NM_000488.4:c.218C>T MANE Select NP_000479.1:p.Pro73Leu
NM_001365052.2:c.74C>T NP_001351981.1:p.Pro25Leu
NM_001386302.1:c.218C>T NP_001373231.1:p.Pro73Leu
NM_001386303.1:c.299C>T NP_001373232.1:p.Pro100Leu
NM_001386304.1:c.218C>T NP_001373233.1:p.Pro73Leu
NM_001386305.1:c.218C>T NP_001373234.1:p.Pro73Leu
NM_001386306.1:c.218C>T NP_001373235.1:p.Pro73Leu