Canonical Allele Identifier: CA343772673

Gene: SERPINC1

Linked Data

• ClinVar Variation Id: 1527888
• ClinVar RCV Id: RCV002074463
• dbSNP Id: rs2102773346
• MyVariant Identifiers: chr1:g.173873191C>G (hg19) ; chr1:g.173904053C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904053C>G , CM000663.2:g.173904053C>G	GRCh38
NC_000001.10:g.173873191C>G , CM000663.1:g.173873191C>G	GRCh37
NC_000001.9:g.172139814C>G	NCBI36
NG_012462.1:g.18326G>C , LRG_577:g.18326G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1231G>C MANE Select	ENSP00000356671.3:p.Gly411Arg
ENST00000367698.3:c.1231G>C	ENSP00000356671.3:p.Gly411Arg
ENST00000617423.4:c.616G>C	ENSP00000478688.1:p.Gly206Arg
NM_000488.3:c.1231G>C , LRG_577t1:c.1231G>C	NP_000479.1:p.Gly411Arg
XM_005245198.2:c.1087G>C	XP_005245255.1:p.Gly363Arg
NM_001365052.1:c.1087G>C	NP_001351981.1:p.Gly363Arg
NM_000488.4:c.1231G>C MANE Select	NP_000479.1:p.Gly411Arg
NM_001365052.2:c.1087G>C	NP_001351981.1:p.Gly363Arg
NM_001386302.1:c.1354G>C	NP_001373231.1:p.Gly452Arg
NM_001386303.1:c.1312G>C	NP_001373232.1:p.Gly438Arg
NM_001386304.1:c.1210G>C	NP_001373233.1:p.Gly404Arg
NM_001386305.1:c.1174G>C	NP_001373234.1:p.Gly392Arg
NM_001386306.1:c.1015G>C	NP_001373235.1:p.Gly339Arg