Canonical Allele Identifier: CA343772600

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873152C>G (hg19) ; chr1:g.173904014C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904014C>G , CM000663.2:g.173904014C>G	GRCh38
NC_000001.10:g.173873152C>G , CM000663.1:g.173873152C>G	GRCh37
NC_000001.9:g.172139775C>G	NCBI36
NG_012462.1:g.18365G>C , LRG_577:g.18365G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1270G>C MANE Select	ENSP00000356671.3:p.Gly424Arg
ENST00000367698.3:c.1270G>C	ENSP00000356671.3:p.Gly424Arg
ENST00000617423.4:c.655G>C	ENSP00000478688.1:p.Gly219Arg
NM_000488.3:c.1270G>C , LRG_577t1:c.1270G>C	NP_000479.1:p.Gly424Arg
XM_005245198.2:c.1126G>C	XP_005245255.1:p.Gly376Arg
NM_001365052.1:c.1126G>C	NP_001351981.1:p.Gly376Arg
NM_000488.4:c.1270G>C MANE Select	NP_000479.1:p.Gly424Arg
NM_001365052.2:c.1126G>C	NP_001351981.1:p.Gly376Arg
NM_001386302.1:c.1393G>C	NP_001373231.1:p.Gly465Arg
NM_001386303.1:c.1351G>C	NP_001373232.1:p.Gly451Arg
NM_001386304.1:c.1249G>C	NP_001373233.1:p.Gly417Arg
NM_001386305.1:c.1213G>C	NP_001373234.1:p.Gly405Arg
NM_001386306.1:c.1054G>C	NP_001373235.1:p.Gly352Arg