Canonical Allele Identifier: CA421821280

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873066A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903928A>T , CM000663.2:g.173903928A>T	GRCh38
NC_000001.10:g.173873066A>T , CM000663.1:g.173873066A>T	GRCh37
NC_000001.9:g.172139689A>T	NCBI36
NG_012462.1:g.18451T>A , LRG_577:g.18451T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1356T>A MANE Select	ENSP00000356671.3:p.Ile452=
ENST00000367698.3:c.1356T>A	ENSP00000356671.3:p.Ile452=
ENST00000617423.4:c.741T>A	ENSP00000478688.1:p.Ile247=
NM_000488.3:c.1356T>A , LRG_577t1:c.1356T>A	NP_000479.1:p.Ile452=
XM_005245198.2:c.1212T>A	XP_005245255.1:p.Ile404=
NM_001365052.1:c.1212T>A	NP_001351981.1:p.Ile404=
NM_000488.4:c.1356T>A MANE Select	NP_000479.1:p.Ile452=
NM_001365052.2:c.1212T>A	NP_001351981.1:p.Ile404=
NM_001386302.1:c.1479T>A	NP_001373231.1:p.Ile493=
NM_001386303.1:c.1437T>A	NP_001373232.1:p.Ile479=
NM_001386304.1:c.1335T>A	NP_001373233.1:p.Ile445=
NM_001386305.1:c.1299T>A	NP_001373234.1:p.Ile433=
NM_001386306.1:c.1140T>A	NP_001373235.1:p.Ile380=