Canonical Allele Identifier: CA343772518

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873134T>A (hg19) ; chr1:g.173903996T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903996T>A , CM000663.2:g.173903996T>A	GRCh38
NC_000001.10:g.173873134T>A , CM000663.1:g.173873134T>A	GRCh37
NC_000001.9:g.172139757T>A	NCBI36
NG_012462.1:g.18383A>T , LRG_577:g.18383A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1288A>T MANE Select	ENSP00000356671.3:p.Asn430Tyr
ENST00000367698.3:c.1288A>T	ENSP00000356671.3:p.Asn430Tyr
ENST00000617423.4:c.673A>T	ENSP00000478688.1:p.Asn225Tyr
NM_000488.3:c.1288A>T , LRG_577t1:c.1288A>T	NP_000479.1:p.Asn430Tyr
XM_005245198.2:c.1144A>T	XP_005245255.1:p.Asn382Tyr
NM_001365052.1:c.1144A>T	NP_001351981.1:p.Asn382Tyr
NM_000488.4:c.1288A>T MANE Select	NP_000479.1:p.Asn430Tyr
NM_001365052.2:c.1144A>T	NP_001351981.1:p.Asn382Tyr
NM_001386302.1:c.1411A>T	NP_001373231.1:p.Asn471Tyr
NM_001386303.1:c.1369A>T	NP_001373232.1:p.Asn457Tyr
NM_001386304.1:c.1267A>T	NP_001373233.1:p.Asn423Tyr
NM_001386305.1:c.1231A>T	NP_001373234.1:p.Asn411Tyr
NM_001386306.1:c.1072A>T	NP_001373235.1:p.Asn358Tyr