Canonical Allele Identifier: CA343772270

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873089T>C (hg19) ; chr1:g.173903951T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903951T>C , CM000663.2:g.173903951T>C	GRCh38
NC_000001.10:g.173873089T>C , CM000663.1:g.173873089T>C	GRCh37
NC_000001.9:g.172139712T>C	NCBI36
NG_012462.1:g.18428A>G , LRG_577:g.18428A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1333A>G MANE Select	ENSP00000356671.3:p.Arg445Gly
ENST00000367698.3:c.1333A>G	ENSP00000356671.3:p.Arg445Gly
ENST00000617423.4:c.718A>G	ENSP00000478688.1:p.Arg240Gly
NM_000488.3:c.1333A>G , LRG_577t1:c.1333A>G	NP_000479.1:p.Arg445Gly
XM_005245198.2:c.1189A>G	XP_005245255.1:p.Arg397Gly
NM_001365052.1:c.1189A>G	NP_001351981.1:p.Arg397Gly
NM_000488.4:c.1333A>G MANE Select	NP_000479.1:p.Arg445Gly
NM_001365052.2:c.1189A>G	NP_001351981.1:p.Arg397Gly
NM_001386302.1:c.1456A>G	NP_001373231.1:p.Arg486Gly
NM_001386303.1:c.1414A>G	NP_001373232.1:p.Arg472Gly
NM_001386304.1:c.1312A>G	NP_001373233.1:p.Arg438Gly
NM_001386305.1:c.1276A>G	NP_001373234.1:p.Arg426Gly
NM_001386306.1:c.1117A>G	NP_001373235.1:p.Arg373Gly