Canonical Allele Identifier: CA2695199917

Gene: SERPINC1

Linked Data

• ClinVar Variation Id: 2631668
• ClinVar RCV Id: RCV003397442

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903926delinsTTAT , CM000663.2:g.173903926delinsTTAT	GRCh38
NC_000001.10:g.173873064delinsTTAT , CM000663.1:g.173873064delinsTTAT	GRCh37
NC_000001.9:g.172139687delinsTTAT	NCBI36
NG_012462.1:g.18453delinsATAA , LRG_577:g.18453delinsATAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1358delinsATAA MANE Select	ENSP00000356671.3:p.Ile453delinsAsnAsn
ENST00000367698.3:c.1358delinsATAA	ENSP00000356671.3:p.Ile453delinsAsnAsn
ENST00000617423.4:c.743delinsATAA	ENSP00000478688.1:p.Ile248delinsAsnAsn
NM_000488.3:c.1358delinsATAA , LRG_577t1:c.1358delinsATAA	NP_000479.1:p.Ile453delinsAsnAsn
XM_005245198.2:c.1214delinsATAA	XP_005245255.1:p.Ile405delinsAsnAsn
NM_001365052.1:c.1214delinsATAA	NP_001351981.1:p.Ile405delinsAsnAsn
NM_000488.4:c.1358delinsATAA MANE Select	NP_000479.1:p.Ile453delinsAsnAsn
NM_001365052.2:c.1214delinsATAA	NP_001351981.1:p.Ile405delinsAsnAsn
NM_001386302.1:c.1481delinsATAA	NP_001373231.1:p.Ile494delinsAsnAsn
NM_001386303.1:c.1439delinsATAA	NP_001373232.1:p.Ile480delinsAsnAsn
NM_001386304.1:c.1337delinsATAA	NP_001373233.1:p.Ile446delinsAsnAsn
NM_001386305.1:c.1301delinsATAA	NP_001373234.1:p.Ile434delinsAsnAsn
NM_001386306.1:c.1142delinsATAA	NP_001373235.1:p.Ile381delinsAsnAsn