Canonical Allele Identifier: CA421821531

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873135G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903997G>T , CM000663.2:g.173903997G>T	GRCh38
NC_000001.10:g.173873135G>T , CM000663.1:g.173873135G>T	GRCh37
NC_000001.9:g.172139758G>T	NCBI36
NG_012462.1:g.18382C>A , LRG_577:g.18382C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1287C>A MANE Select	ENSP00000356671.3:p.Pro429=
ENST00000367698.3:c.1287C>A	ENSP00000356671.3:p.Pro429=
ENST00000617423.4:c.672C>A	ENSP00000478688.1:p.Pro224=
NM_000488.3:c.1287C>A , LRG_577t1:c.1287C>A	NP_000479.1:p.Pro429=
XM_005245198.2:c.1143C>A	XP_005245255.1:p.Pro381=
NM_001365052.1:c.1143C>A	NP_001351981.1:p.Pro381=
NM_000488.4:c.1287C>A MANE Select	NP_000479.1:p.Pro429=
NM_001365052.2:c.1143C>A	NP_001351981.1:p.Pro381=
NM_001386302.1:c.1410C>A	NP_001373231.1:p.Pro470=
NM_001386303.1:c.1368C>A	NP_001373232.1:p.Pro456=
NM_001386304.1:c.1266C>A	NP_001373233.1:p.Pro422=
NM_001386305.1:c.1230C>A	NP_001373234.1:p.Pro410=
NM_001386306.1:c.1071C>A	NP_001373235.1:p.Pro357=