Canonical Allele Identifier: CA421942765

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173879012C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909874C>T , CM000663.2:g.173909874C>T	GRCh38
NC_000001.10:g.173879012C>T , CM000663.1:g.173879012C>T	GRCh37
NC_000001.9:g.172145635C>T	NCBI36
NG_012462.1:g.12505G>A , LRG_577:g.12505G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.831G>A MANE Select	ENSP00000356671.3:p.Glu277=
ENST00000367698.3:c.831G>A	ENSP00000356671.3:p.Glu277=
ENST00000487183.1:n.482G>A
ENST00000617423.4:c.559+1990G>A	ENSP00000478688.1:n.559+1990G>A
NM_000488.3:c.831G>A , LRG_577t1:c.831G>A	NP_000479.1:p.Glu277=
XM_005245198.2:c.687G>A	XP_005245255.1:p.Glu229=
NM_001365052.1:c.687G>A	NP_001351981.1:p.Glu229=
NM_000488.4:c.831G>A MANE Select	NP_000479.1:p.Glu277=
NM_001365052.2:c.687G>A	NP_001351981.1:p.Glu229=
NM_001386302.1:c.954G>A	NP_001373231.1:p.Glu318=
NM_001386303.1:c.912G>A	NP_001373232.1:p.Glu304=
NM_001386304.1:c.810G>A	NP_001373233.1:p.Glu270=
NM_001386305.1:c.774G>A	NP_001373234.1:p.Glu258=
NM_001386306.1:c.615G>A	NP_001373235.1:p.Glu205=