Canonical Allele Identifier: CA421942808
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1483715794

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909913C>T , CM000663.2:g.173909913C>T GRCh38
NC_000001.10:g.173879051C>T , CM000663.1:g.173879051C>T GRCh37
NC_000001.9:g.172145674C>T NCBI36
NG_012462.1:g.12466G>A , LRG_577:g.12466G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.792G>A MANE Select ENSP00000356671.3:p.Glu264=
ENST00000367698.3:c.792G>A ENSP00000356671.3:p.Glu264=
ENST00000487183.1:n.443G>A
ENST00000617423.4:c.559+1951G>A ENSP00000478688.1:n.559+1951G>A
NM_000488.3:c.792G>A , LRG_577t1:c.792G>A NP_000479.1:p.Glu264=
XM_005245198.2:c.648G>A XP_005245255.1:p.Glu216=
NM_001365052.1:c.648G>A NP_001351981.1:p.Glu216=
NM_000488.4:c.792G>A MANE Select NP_000479.1:p.Glu264=
NM_001365052.2:c.648G>A NP_001351981.1:p.Glu216=
NM_001386302.1:c.915G>A NP_001373231.1:p.Glu305=
NM_001386303.1:c.873G>A NP_001373232.1:p.Glu291=
NM_001386304.1:c.771G>A NP_001373233.1:p.Glu257=
NM_001386305.1:c.763-28G>A NP_001373234.1:n.763-28G>A
NM_001386306.1:c.576G>A NP_001373235.1:p.Glu192=