Canonical Allele Identifier: CA343772309

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873097A>C (hg19) ; chr1:g.173903959A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903959A>C , CM000663.2:g.173903959A>C	GRCh38
NC_000001.10:g.173873097A>C , CM000663.1:g.173873097A>C	GRCh37
NC_000001.9:g.172139720A>C	NCBI36
NG_012462.1:g.18420T>G , LRG_577:g.18420T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1325T>G MANE Select	ENSP00000356671.3:p.Val442Gly
ENST00000367698.3:c.1325T>G	ENSP00000356671.3:p.Val442Gly
ENST00000617423.4:c.710T>G	ENSP00000478688.1:p.Val237Gly
NM_000488.3:c.1325T>G , LRG_577t1:c.1325T>G	NP_000479.1:p.Val442Gly
XM_005245198.2:c.1181T>G	XP_005245255.1:p.Val394Gly
NM_001365052.1:c.1181T>G	NP_001351981.1:p.Val394Gly
NM_000488.4:c.1325T>G MANE Select	NP_000479.1:p.Val442Gly
NM_001365052.2:c.1181T>G	NP_001351981.1:p.Val394Gly
NM_001386302.1:c.1448T>G	NP_001373231.1:p.Val483Gly
NM_001386303.1:c.1406T>G	NP_001373232.1:p.Val469Gly
NM_001386304.1:c.1304T>G	NP_001373233.1:p.Val435Gly
NM_001386305.1:c.1268T>G	NP_001373234.1:p.Val423Gly
NM_001386306.1:c.1109T>G	NP_001373235.1:p.Val370Gly