Canonical Allele Identifier: CA343772352

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873104A>C (hg19) ; chr1:g.173903966A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903966A>C , CM000663.2:g.173903966A>C	GRCh38
NC_000001.10:g.173873104A>C , CM000663.1:g.173873104A>C	GRCh37
NC_000001.9:g.172139727A>C	NCBI36
NG_012462.1:g.18413T>G , LRG_577:g.18413T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1318T>G MANE Select	ENSP00000356671.3:p.Phe440Val
ENST00000367698.3:c.1318T>G	ENSP00000356671.3:p.Phe440Val
ENST00000617423.4:c.703T>G	ENSP00000478688.1:p.Phe235Val
NM_000488.3:c.1318T>G , LRG_577t1:c.1318T>G	NP_000479.1:p.Phe440Val
XM_005245198.2:c.1174T>G	XP_005245255.1:p.Phe392Val
NM_001365052.1:c.1174T>G	NP_001351981.1:p.Phe392Val
NM_000488.4:c.1318T>G MANE Select	NP_000479.1:p.Phe440Val
NM_001365052.2:c.1174T>G	NP_001351981.1:p.Phe392Val
NM_001386302.1:c.1441T>G	NP_001373231.1:p.Phe481Val
NM_001386303.1:c.1399T>G	NP_001373232.1:p.Phe467Val
NM_001386304.1:c.1297T>G	NP_001373233.1:p.Phe433Val
NM_001386305.1:c.1261T>G	NP_001373234.1:p.Phe421Val
NM_001386306.1:c.1102T>G	NP_001373235.1:p.Phe368Val