Canonical Allele Identifier: CA421943252

Gene: SERPINC1

Linked Data

• ClinVar Variation Id: 2709550
• ClinVar RCV Id: RCV003525748
• dbSNP Id: rs1443804575
• gnomAD v4: 1-173914856-G-A
• MyVariant Identifiers: chr1:g.173883994G>A (hg19) ; chr1:g.173914856G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173914856G>A , CM000663.2:g.173914856G>A	GRCh38
NC_000001.10:g.173883994G>A , CM000663.1:g.173883994G>A	GRCh37
NC_000001.9:g.172150617G>A	NCBI36
NG_012462.1:g.7523C>T , LRG_577:g.7523C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.105C>T MANE Select	ENSP00000356671.3:p.Ser35=
ENST00000367698.3:c.105C>T	ENSP00000356671.3:p.Ser35=
ENST00000494024.1:n.331C>T
ENST00000617423.4:c.105C>T	ENSP00000478688.1:p.Ser35=
NM_000488.3:c.105C>T , LRG_577t1:c.105C>T	NP_000479.1:p.Ser35=
XM_005245198.2:c.-40C>T	XP_005245255.1:n.-40C>T
NM_001365052.1:c.-40C>T	NP_001351981.1:n.-40C>T
NM_000488.4:c.105C>T MANE Select	NP_000479.1:p.Ser35=
NM_001365052.2:c.-40C>T	NP_001351981.1:n.-40C>T
NM_001386302.1:c.105C>T	NP_001373231.1:p.Ser35=
NM_001386303.1:c.186C>T	NP_001373232.1:p.Ser62=
NM_001386304.1:c.105C>T	NP_001373233.1:p.Ser35=
NM_001386305.1:c.105C>T	NP_001373234.1:p.Ser35=
NM_001386306.1:c.105C>T	NP_001373235.1:p.Ser35=