Canonical Allele Identifier: CA343772573

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873143G>T (hg19) ; chr1:g.173904005G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904005G>T , CM000663.2:g.173904005G>T	GRCh38
NC_000001.10:g.173873143G>T , CM000663.1:g.173873143G>T	GRCh37
NC_000001.9:g.172139766G>T	NCBI36
NG_012462.1:g.18374C>A , LRG_577:g.18374C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1279C>A MANE Select	ENSP00000356671.3:p.Leu427Ile
ENST00000367698.3:c.1279C>A	ENSP00000356671.3:p.Leu427Ile
ENST00000617423.4:c.664C>A	ENSP00000478688.1:p.Leu222Ile
NM_000488.3:c.1279C>A , LRG_577t1:c.1279C>A	NP_000479.1:p.Leu427Ile
XM_005245198.2:c.1135C>A	XP_005245255.1:p.Leu379Ile
NM_001365052.1:c.1135C>A	NP_001351981.1:p.Leu379Ile
NM_000488.4:c.1279C>A MANE Select	NP_000479.1:p.Leu427Ile
NM_001365052.2:c.1135C>A	NP_001351981.1:p.Leu379Ile
NM_001386302.1:c.1402C>A	NP_001373231.1:p.Leu468Ile
NM_001386303.1:c.1360C>A	NP_001373232.1:p.Leu454Ile
NM_001386304.1:c.1258C>A	NP_001373233.1:p.Leu420Ile
NM_001386305.1:c.1222C>A	NP_001373234.1:p.Leu408Ile
NM_001386306.1:c.1063C>A	NP_001373235.1:p.Leu355Ile