Canonical Allele Identifier: CA2573051423
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1321893
ClinVar RCV Id: RCV001779977

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173912552_173914879del , CM000663.2:g.173912552_173914879del GRCh38
NC_000001.10:g.173881690_173884017del , CM000663.1:g.173881690_173884017del GRCh37
NC_000001.9:g.172148313_172150640del NCBI36
NG_012462.1:g.7502_9829del , LRG_577:g.7502_9829del

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.84_409-536del
ENST00000367698.3:c.84_409-536del
ENST00000494024.1:n.310_635-536del
ENST00000617423.4:c.84_409-536del
NM_000488.3:c.84_409-536del , LRG_577t1:c.84_409-536del
XM_005245198.2:c.-61_265-536del
NM_001365052.1:c.-61_265-536del
NM_000488.4:c.84_409-536del
NM_001365052.2:c.-61_265-536del
NM_001386302.1:c.84_409-536del
NM_001386303.1:c.165_490-536del
NM_001386304.1:c.84_409-536del
NM_001386305.1:c.84_409-536del
NM_001386306.1:c.84_409-1659del