Canonical Allele Identifier: CA343772662

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873186A>T (hg19) ; chr1:g.173904048A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904048A>T , CM000663.2:g.173904048A>T	GRCh38
NC_000001.10:g.173873186A>T , CM000663.1:g.173873186A>T	GRCh37
NC_000001.9:g.172139809A>T	NCBI36
NG_012462.1:g.18331T>A , LRG_577:g.18331T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1236T>A MANE Select	ENSP00000356671.3:p.Ser412Arg
ENST00000367698.3:c.1236T>A	ENSP00000356671.3:p.Ser412Arg
ENST00000617423.4:c.621T>A	ENSP00000478688.1:p.Ser207Arg
NM_000488.3:c.1236T>A , LRG_577t1:c.1236T>A	NP_000479.1:p.Ser412Arg
XM_005245198.2:c.1092T>A	XP_005245255.1:p.Ser364Arg
NM_001365052.1:c.1092T>A	NP_001351981.1:p.Ser364Arg
NM_000488.4:c.1236T>A MANE Select	NP_000479.1:p.Ser412Arg
NM_001365052.2:c.1092T>A	NP_001351981.1:p.Ser364Arg
NM_001386302.1:c.1359T>A	NP_001373231.1:p.Ser453Arg
NM_001386303.1:c.1317T>A	NP_001373232.1:p.Ser439Arg
NM_001386304.1:c.1215T>A	NP_001373233.1:p.Ser405Arg
NM_001386305.1:c.1179T>A	NP_001373234.1:p.Ser393Arg
NM_001386306.1:c.1020T>A	NP_001373235.1:p.Ser340Arg