Canonical Allele Identifier: CA343773929

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878845G>C (hg19) ; chr1:g.173909707G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909707G>C , CM000663.2:g.173909707G>C	GRCh38
NC_000001.10:g.173878845G>C , CM000663.1:g.173878845G>C	GRCh37
NC_000001.9:g.172145468G>C	NCBI36
NG_012462.1:g.12672C>G , LRG_577:g.12672C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.998C>G MANE Select	ENSP00000356671.3:p.Pro333Arg
ENST00000367698.3:c.998C>G	ENSP00000356671.3:p.Pro333Arg
ENST00000617423.4:c.559+2157C>G	ENSP00000478688.1:n.559+2157C>G
NM_000488.3:c.998C>G , LRG_577t1:c.998C>G	NP_000479.1:p.Pro333Arg
XM_005245198.2:c.854C>G	XP_005245255.1:p.Pro285Arg
NM_001365052.1:c.854C>G	NP_001351981.1:p.Pro285Arg
NM_000488.4:c.998C>G MANE Select	NP_000479.1:p.Pro333Arg
NM_001365052.2:c.854C>G	NP_001351981.1:p.Pro285Arg
NM_001386302.1:c.1121C>G	NP_001373231.1:p.Pro374Arg
NM_001386303.1:c.1079C>G	NP_001373232.1:p.Pro360Arg
NM_001386304.1:c.977C>G	NP_001373233.1:p.Pro326Arg
NM_001386305.1:c.941C>G	NP_001373234.1:p.Pro314Arg
NM_001386306.1:c.782C>G	NP_001373235.1:p.Pro261Arg