Canonical Allele Identifier: CA2573051421
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1321894
ClinVar RCV Id: RCV001779978

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173910345_173913622del , CM000663.2:g.173910345_173913622del GRCh38
NC_000001.10:g.173879483_173882760del , CM000663.1:g.173879483_173882760del GRCh37
NC_000001.9:g.172146106_172149383del NCBI36
NG_012462.1:g.8774_12051del , LRG_577:g.8774_12051del

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.408+948_763-386del
ENST00000367698.3:c.408+948_763-386del
ENST00000487183.1:n.113+948_414-386del
ENST00000617423.4:c.408+948_559+1536del
NM_000488.3:c.408+948_763-386del , LRG_577t1:c.408+948_763-386del
XM_005245198.2:c.264+948_619-386del
NM_001365052.1:c.264+948_619-386del
NM_000488.4:c.408+948_763-386del
NM_001365052.2:c.264+948_619-386del
NM_001386302.1:c.408+948_885+303del
NM_001386303.1:c.489+948_844-386del
NM_001386304.1:c.408+948_742-386del
NM_001386305.1:c.408+948_762+426del
NM_001386306.1:c.408+948_547-386del