Canonical Allele Identifier: CA421942727

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878940C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909802C>T , CM000663.2:g.173909802C>T	GRCh38
NC_000001.10:g.173878940C>T , CM000663.1:g.173878940C>T	GRCh37
NC_000001.9:g.172145563C>T	NCBI36
NG_012462.1:g.12577G>A , LRG_577:g.12577G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.903G>A MANE Select	ENSP00000356671.3:p.Val301=
ENST00000367698.3:c.903G>A	ENSP00000356671.3:p.Val301=
ENST00000487183.1:n.554G>A
ENST00000617423.4:c.559+2062G>A	ENSP00000478688.1:n.559+2062G>A
NM_000488.3:c.903G>A , LRG_577t1:c.903G>A	NP_000479.1:p.Val301=
XM_005245198.2:c.759G>A	XP_005245255.1:p.Val253=
NM_001365052.1:c.759G>A	NP_001351981.1:p.Val253=
NM_000488.4:c.903G>A MANE Select	NP_000479.1:p.Val301=
NM_001365052.2:c.759G>A	NP_001351981.1:p.Val253=
NM_001386302.1:c.1026G>A	NP_001373231.1:p.Val342=
NM_001386303.1:c.984G>A	NP_001373232.1:p.Val328=
NM_001386304.1:c.882G>A	NP_001373233.1:p.Val294=
NM_001386305.1:c.846G>A	NP_001373234.1:p.Val282=
NM_001386306.1:c.687G>A	NP_001373235.1:p.Val229=