Canonical Allele Identifier: CA421823465

Gene: SERPINC1

Linked Data

• ClinVar Variation Id: 2098360
• ClinVar RCV Id: RCV003030907
• MyVariant Identifiers: chr1:g.173886377T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173917239T>A , CM000663.2:g.173917239T>A	GRCh38
NC_000001.10:g.173886377T>A , CM000663.1:g.173886377T>A	GRCh37
NC_000001.9:g.172153000T>A	NCBI36
NG_012462.1:g.5140A>T , LRG_577:g.5140A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.21A>T MANE Select	ENSP00000356671.3:p.Gly7=
ENST00000367698.3:c.21A>T	ENSP00000356671.3:p.Gly7=
ENST00000494024.1:n.78A>T
ENST00000617423.4:c.21A>T	ENSP00000478688.1:p.Gly7=
NM_000488.3:c.21A>T , LRG_577t1:c.21A>T	NP_000479.1:p.Gly7=
XM_005245198.2:c.-293A>T	XP_005245255.1:n.-293A>T
NM_001365052.1:c.-293A>T	NP_001351981.1:n.-293A>T
NM_000488.4:c.21A>T MANE Select	NP_000479.1:p.Gly7=
NM_001365052.2:c.-293A>T	NP_001351981.1:n.-293A>T
NM_001386302.1:c.21A>T	NP_001373231.1:p.Gly7=
NM_001386303.1:c.21A>T	NP_001373232.1:p.Gly7=
NM_001386304.1:c.21A>T	NP_001373233.1:p.Gly7=
NM_001386305.1:c.21A>T	NP_001373234.1:p.Gly7=
NM_001386306.1:c.21A>T	NP_001373235.1:p.Gly7=