Canonical Allele Identifier: CA421942790

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878709A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909571A>T , CM000663.2:g.173909571A>T	GRCh38
NC_000001.10:g.173878709A>T , CM000663.1:g.173878709A>T	GRCh37
NC_000001.9:g.172145332A>T	NCBI36
NG_012462.1:g.12808T>A , LRG_577:g.12808T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1134T>A MANE Select	ENSP00000356671.3:p.Pro378=
ENST00000367698.3:c.1134T>A	ENSP00000356671.3:p.Pro378=
ENST00000617423.4:c.560-2078T>A	ENSP00000478688.1:n.560-2078T>A
NM_000488.3:c.1134T>A , LRG_577t1:c.1134T>A	NP_000479.1:p.Pro378=
XM_005245198.2:c.990T>A	XP_005245255.1:p.Pro330=
NM_001365052.1:c.990T>A	NP_001351981.1:p.Pro330=
NM_000488.4:c.1134T>A MANE Select	NP_000479.1:p.Pro378=
NM_001365052.2:c.990T>A	NP_001351981.1:p.Pro330=
NM_001386302.1:c.1257T>A	NP_001373231.1:p.Pro419=
NM_001386303.1:c.1215T>A	NP_001373232.1:p.Pro405=
NM_001386304.1:c.1113T>A	NP_001373233.1:p.Pro371=
NM_001386305.1:c.1077T>A	NP_001373234.1:p.Pro359=
NM_001386306.1:c.918T>A	NP_001373235.1:p.Pro306=