Canonical Allele Identifier: CA343772014

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873035C>T (hg19) ; chr1:g.173903897C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903897C>T , CM000663.2:g.173903897C>T	GRCh38
NC_000001.10:g.173873035C>T , CM000663.1:g.173873035C>T	GRCh37
NC_000001.9:g.172139658C>T	NCBI36
NG_012462.1:g.18482G>A , LRG_577:g.18482G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1387G>A MANE Select	ENSP00000356671.3:p.Val463Ile
ENST00000367698.3:c.1387G>A	ENSP00000356671.3:p.Val463Ile
ENST00000617423.4:c.772G>A	ENSP00000478688.1:p.Val258Ile
NM_000488.3:c.1387G>A , LRG_577t1:c.1387G>A	NP_000479.1:p.Val463Ile
XM_005245198.2:c.1243G>A	XP_005245255.1:p.Val415Ile
NM_001365052.1:c.1243G>A	NP_001351981.1:p.Val415Ile
NM_000488.4:c.1387G>A MANE Select	NP_000479.1:p.Val463Ile
NM_001365052.2:c.1243G>A	NP_001351981.1:p.Val415Ile
NM_001386302.1:c.1510G>A	NP_001373231.1:p.Val504Ile
NM_001386303.1:c.1468G>A	NP_001373232.1:p.Val490Ile
NM_001386304.1:c.1366G>A	NP_001373233.1:p.Val456Ile
NM_001386305.1:c.1330G>A	NP_001373234.1:p.Val444Ile
NM_001386306.1:c.1171G>A	NP_001373235.1:p.Val391Ile