Canonical Allele Identifier: CA421821498

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873108C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903970C>T , CM000663.2:g.173903970C>T	GRCh38
NC_000001.10:g.173873108C>T , CM000663.1:g.173873108C>T	GRCh37
NC_000001.9:g.172139731C>T	NCBI36
NG_012462.1:g.18409G>A , LRG_577:g.18409G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1314G>A MANE Select	ENSP00000356671.3:p.Arg438=
ENST00000367698.3:c.1314G>A	ENSP00000356671.3:p.Arg438=
ENST00000617423.4:c.699G>A	ENSP00000478688.1:p.Arg233=
NM_000488.3:c.1314G>A , LRG_577t1:c.1314G>A	NP_000479.1:p.Arg438=
XM_005245198.2:c.1170G>A	XP_005245255.1:p.Arg390=
NM_001365052.1:c.1170G>A	NP_001351981.1:p.Arg390=
NM_000488.4:c.1314G>A MANE Select	NP_000479.1:p.Arg438=
NM_001365052.2:c.1170G>A	NP_001351981.1:p.Arg390=
NM_001386302.1:c.1437G>A	NP_001373231.1:p.Arg479=
NM_001386303.1:c.1395G>A	NP_001373232.1:p.Arg465=
NM_001386304.1:c.1293G>A	NP_001373233.1:p.Arg431=
NM_001386305.1:c.1257G>A	NP_001373234.1:p.Arg419=
NM_001386306.1:c.1098G>A	NP_001373235.1:p.Arg366=