Canonical Allele Identifier: CA343774707

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173879031A>T (hg19) ; chr1:g.173909893A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909893A>T , CM000663.2:g.173909893A>T	GRCh38
NC_000001.10:g.173879031A>T , CM000663.1:g.173879031A>T	GRCh37
NC_000001.9:g.172145654A>T	NCBI36
NG_012462.1:g.12486T>A , LRG_577:g.12486T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.812T>A MANE Select	ENSP00000356671.3:p.Phe271Tyr
ENST00000367698.3:c.812T>A	ENSP00000356671.3:p.Phe271Tyr
ENST00000487183.1:n.463T>A
ENST00000617423.4:c.559+1971T>A	ENSP00000478688.1:n.559+1971T>A
NM_000488.3:c.812T>A , LRG_577t1:c.812T>A	NP_000479.1:p.Phe271Tyr
XM_005245198.2:c.668T>A	XP_005245255.1:p.Phe223Tyr
NM_001365052.1:c.668T>A	NP_001351981.1:p.Phe223Tyr
NM_000488.4:c.812T>A MANE Select	NP_000479.1:p.Phe271Tyr
NM_001365052.2:c.668T>A	NP_001351981.1:p.Phe223Tyr
NM_001386302.1:c.935T>A	NP_001373231.1:p.Phe312Tyr
NM_001386303.1:c.893T>A	NP_001373232.1:p.Phe298Tyr
NM_001386304.1:c.791T>A	NP_001373233.1:p.Phe264Tyr
NM_001386305.1:c.763-8T>A	NP_001373234.1:n.763-8T>A
NM_001386306.1:c.596T>A	NP_001373235.1:p.Phe199Tyr