Canonical Allele Identifier: CA915943679

Gene: SERPINC1

Linked Data

• ClinVar Variation Id: 627245
• ClinVar RCV Id: RCV000852036
• dbSNP Id: rs1572092103

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173914806del , CM000663.2:g.173914806del	GRCh38
NC_000001.10:g.173883944del , CM000663.1:g.173883944del	GRCh37
NC_000001.9:g.172150567del	NCBI36
NG_012462.1:g.7573del , LRG_577:g.7573del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.155del MANE Select	ENSP00000356671.3:p.Met52SerfsTer?
ENST00000367698.3:c.155del	ENSP00000356671.3:p.Met52SerfsTer?
ENST00000494024.1:n.381del
ENST00000617423.4:c.155del	ENSP00000478688.1:p.Met52SerfsTer?
NM_000488.3:c.155del , LRG_577t1:c.155del	NP_000479.1:p.Met52SerfsTer?
XM_005245198.2:c.11del	XP_005245255.1:p.Met4SerfsTer?
NM_001365052.1:c.11del	NP_001351981.1:p.Met4SerfsTer?
NM_000488.4:c.155del MANE Select	NP_000479.1:p.Met52SerfsTer?
NM_001365052.2:c.11del	NP_001351981.1:p.Met4SerfsTer?
NM_001386302.1:c.155del	NP_001373231.1:p.Met52SerfsTer?
NM_001386303.1:c.236del	NP_001373232.1:p.Met79SerfsTer?
NM_001386304.1:c.155del	NP_001373233.1:p.Met52SerfsTer?
NM_001386305.1:c.155del	NP_001373234.1:p.Met52SerfsTer?
NM_001386306.1:c.155del	NP_001373235.1:p.Met52SerfsTer?