Canonical Allele Identifier: CA421942784

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1657671913
• gnomAD v3: 1-173909565-C-T
• gnomAD v4: 1-173909565-C-T
• MyVariant Identifiers: chr1:g.173878703C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909565C>T , CM000663.2:g.173909565C>T	GRCh38
NC_000001.10:g.173878703C>T , CM000663.1:g.173878703C>T	GRCh37
NC_000001.9:g.172145326C>T	NCBI36
NG_012462.1:g.12814G>A , LRG_577:g.12814G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1140G>A MANE Select	ENSP00000356671.3:p.Lys380=
ENST00000367698.3:c.1140G>A	ENSP00000356671.3:p.Lys380=
ENST00000617423.4:c.560-2072G>A	ENSP00000478688.1:n.560-2072G>A
NM_000488.3:c.1140G>A , LRG_577t1:c.1140G>A	NP_000479.1:p.Lys380=
XM_005245198.2:c.996G>A	XP_005245255.1:p.Lys332=
NM_001365052.1:c.996G>A	NP_001351981.1:p.Lys332=
NM_000488.4:c.1140G>A MANE Select	NP_000479.1:p.Lys380=
NM_001365052.2:c.996G>A	NP_001351981.1:p.Lys332=
NM_001386302.1:c.1263G>A	NP_001373231.1:p.Lys421=
NM_001386303.1:c.1221G>A	NP_001373232.1:p.Lys407=
NM_001386304.1:c.1119G>A	NP_001373233.1:p.Lys373=
NM_001386305.1:c.1083G>A	NP_001373234.1:p.Lys361=
NM_001386306.1:c.924G>A	NP_001373235.1:p.Lys308=