Canonical Allele Identifier: CA2739275404

Gene: SERPINC1

Linked Data

• ClinVar Variation Id: 2777095
• ClinVar RCV Id: RCV003638986

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173914863dup , CM000663.2:g.173914863dup	GRCh38
NC_000001.10:g.173884001dup , CM000663.1:g.173884001dup	GRCh37
NC_000001.9:g.172150624dup	NCBI36
NG_012462.1:g.7516dup , LRG_577:g.7516dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.98dup MANE Select	ENSP00000356671.3:p.His33GlnfsTer?
ENST00000367698.3:c.98dup	ENSP00000356671.3:p.His33GlnfsTer?
ENST00000494024.1:n.324dup
ENST00000617423.4:c.98dup	ENSP00000478688.1:p.His33GlnfsTer?
NM_000488.3:c.98dup , LRG_577t1:c.98dup	NP_000479.1:p.His33GlnfsTer?
XM_005245198.2:c.-47dup	XP_005245255.1:n.-47dup
NM_001365052.1:c.-47dup	NP_001351981.1:n.-47dup
NM_000488.4:c.98dup MANE Select	NP_000479.1:p.His33GlnfsTer?
NM_001365052.2:c.-47dup	NP_001351981.1:n.-47dup
NM_001386302.1:c.98dup	NP_001373231.1:p.His33GlnfsTer?
NM_001386303.1:c.179dup	NP_001373232.1:p.His60GlnfsTer?
NM_001386304.1:c.98dup	NP_001373233.1:p.His33GlnfsTer?
NM_001386305.1:c.98dup	NP_001373234.1:p.His33GlnfsTer?
NM_001386306.1:c.98dup	NP_001373235.1:p.His33GlnfsTer?