Canonical Allele Identifier: CA421821587

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873165A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904027A>C , CM000663.2:g.173904027A>C	GRCh38
NC_000001.10:g.173873165A>C , CM000663.1:g.173873165A>C	GRCh37
NC_000001.9:g.172139788A>C	NCBI36
NG_012462.1:g.18352T>G , LRG_577:g.18352T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1257T>G MANE Select	ENSP00000356671.3:p.Ala419=
ENST00000367698.3:c.1257T>G	ENSP00000356671.3:p.Ala419=
ENST00000617423.4:c.642T>G	ENSP00000478688.1:p.Ala214=
NM_000488.3:c.1257T>G , LRG_577t1:c.1257T>G	NP_000479.1:p.Ala419=
XM_005245198.2:c.1113T>G	XP_005245255.1:p.Ala371=
NM_001365052.1:c.1113T>G	NP_001351981.1:p.Ala371=
NM_000488.4:c.1257T>G MANE Select	NP_000479.1:p.Ala419=
NM_001365052.2:c.1113T>G	NP_001351981.1:p.Ala371=
NM_001386302.1:c.1380T>G	NP_001373231.1:p.Ala460=
NM_001386303.1:c.1338T>G	NP_001373232.1:p.Ala446=
NM_001386304.1:c.1236T>G	NP_001373233.1:p.Ala412=
NM_001386305.1:c.1200T>G	NP_001373234.1:p.Ala400=
NM_001386306.1:c.1041T>G	NP_001373235.1:p.Ala347=