Canonical Allele Identifier: CA421823122

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173881078T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911940T>C , CM000663.2:g.173911940T>C	GRCh38
NC_000001.10:g.173881078T>C , CM000663.1:g.173881078T>C	GRCh37
NC_000001.9:g.172147701T>C	NCBI36
NG_012462.1:g.10439A>G , LRG_577:g.10439A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.483A>G MANE Select	ENSP00000356671.3:p.Arg161=
ENST00000367698.3:c.483A>G	ENSP00000356671.3:p.Arg161=
ENST00000487183.1:n.188A>G
ENST00000617423.4:c.483A>G	ENSP00000478688.1:p.Arg161=
NM_000488.3:c.483A>G , LRG_577t1:c.483A>G	NP_000479.1:p.Arg161=
XM_005245198.2:c.339A>G	XP_005245255.1:p.Arg113=
NM_001365052.1:c.339A>G	NP_001351981.1:p.Arg113=
NM_000488.4:c.483A>G MANE Select	NP_000479.1:p.Arg161=
NM_001365052.2:c.339A>G	NP_001351981.1:p.Arg113=
NM_001386302.1:c.483A>G	NP_001373231.1:p.Arg161=
NM_001386303.1:c.564A>G	NP_001373232.1:p.Arg188=
NM_001386304.1:c.483A>G	NP_001373233.1:p.Arg161=
NM_001386305.1:c.483A>G	NP_001373234.1:p.Arg161=
NM_001386306.1:c.409-1049A>G	NP_001373235.1:n.409-1049A>G