Canonical Allele Identifier: CA343776818
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173911986T>A , CM000663.2:g.173911986T>A GRCh38
NC_000001.10:g.173881124T>A , CM000663.1:g.173881124T>A GRCh37
NC_000001.9:g.172147747T>A NCBI36
NG_012462.1:g.10393A>T , LRG_577:g.10393A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.437A>T MANE Select ENSP00000356671.3:p.Lys146Ile
ENST00000367698.3:c.437A>T ENSP00000356671.3:p.Lys146Ile
ENST00000487183.1:n.142A>T
ENST00000494024.1:n.663A>T
ENST00000617423.4:c.437A>T ENSP00000478688.1:p.Lys146Ile
NM_000488.3:c.437A>T , LRG_577t1:c.437A>T NP_000479.1:p.Lys146Ile
XM_005245198.2:c.293A>T XP_005245255.1:p.Lys98Ile
NM_001365052.1:c.293A>T NP_001351981.1:p.Lys98Ile
NM_000488.4:c.437A>T MANE Select NP_000479.1:p.Lys146Ile
NM_001365052.2:c.293A>T NP_001351981.1:p.Lys98Ile
NM_001386302.1:c.437A>T NP_001373231.1:p.Lys146Ile
NM_001386303.1:c.518A>T NP_001373232.1:p.Lys173Ile
NM_001386304.1:c.437A>T NP_001373233.1:p.Lys146Ile
NM_001386305.1:c.437A>T NP_001373234.1:p.Lys146Ile
NM_001386306.1:c.409-1095A>T NP_001373235.1:n.409-1095A>T