Canonical Allele Identifier: CA343777996

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173883892T>A (hg19) ; chr1:g.173914754T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173914754T>A , CM000663.2:g.173914754T>A	GRCh38
NC_000001.10:g.173883892T>A , CM000663.1:g.173883892T>A	GRCh37
NC_000001.9:g.172150515T>A	NCBI36
NG_012462.1:g.7625A>T , LRG_577:g.7625A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.207A>T MANE Select	ENSP00000356671.3:p.Glu69Asp
ENST00000367698.3:c.207A>T	ENSP00000356671.3:p.Glu69Asp
ENST00000494024.1:n.433A>T
ENST00000617423.4:c.207A>T	ENSP00000478688.1:p.Glu69Asp
NM_000488.3:c.207A>T , LRG_577t1:c.207A>T	NP_000479.1:p.Glu69Asp
XM_005245198.2:c.63A>T	XP_005245255.1:p.Glu21Asp
NM_001365052.1:c.63A>T	NP_001351981.1:p.Glu21Asp
NM_000488.4:c.207A>T MANE Select	NP_000479.1:p.Glu69Asp
NM_001365052.2:c.63A>T	NP_001351981.1:p.Glu21Asp
NM_001386302.1:c.207A>T	NP_001373231.1:p.Glu69Asp
NM_001386303.1:c.288A>T	NP_001373232.1:p.Glu96Asp
NM_001386304.1:c.207A>T	NP_001373233.1:p.Glu69Asp
NM_001386305.1:c.207A>T	NP_001373234.1:p.Glu69Asp
NM_001386306.1:c.207A>T	NP_001373235.1:p.Glu69Asp