Canonical Allele Identifier: CA343772004

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873034A>T (hg19) ; chr1:g.173903896A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903896A>T , CM000663.2:g.173903896A>T	GRCh38
NC_000001.10:g.173873034A>T , CM000663.1:g.173873034A>T	GRCh37
NC_000001.9:g.172139657A>T	NCBI36
NG_012462.1:g.18483T>A , LRG_577:g.18483T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1388T>A MANE Select	ENSP00000356671.3:p.Val463Asp
ENST00000367698.3:c.1388T>A	ENSP00000356671.3:p.Val463Asp
ENST00000617423.4:c.773T>A	ENSP00000478688.1:p.Val258Asp
NM_000488.3:c.1388T>A , LRG_577t1:c.1388T>A	NP_000479.1:p.Val463Asp
XM_005245198.2:c.1244T>A	XP_005245255.1:p.Val415Asp
NM_001365052.1:c.1244T>A	NP_001351981.1:p.Val415Asp
NM_000488.4:c.1388T>A MANE Select	NP_000479.1:p.Val463Asp
NM_001365052.2:c.1244T>A	NP_001351981.1:p.Val415Asp
NM_001386302.1:c.1511T>A	NP_001373231.1:p.Val504Asp
NM_001386303.1:c.1469T>A	NP_001373232.1:p.Val490Asp
NM_001386304.1:c.1367T>A	NP_001373233.1:p.Val456Asp
NM_001386305.1:c.1331T>A	NP_001373234.1:p.Val444Asp
NM_001386306.1:c.1172T>A	NP_001373235.1:p.Val391Asp