Canonical Allele Identifier: CA343774705

Gene: SERPINC1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.812T>C MANE Select	ENSP00000356671.3:p.Phe271Ser
ENST00000367698.3:c.812T>C	ENSP00000356671.3:p.Phe271Ser
ENST00000487183.1:n.463T>C
ENST00000617423.4:c.559+1971T>C	ENSP00000478688.1:n.559+1971T>C
NM_000488.3:c.812T>C , LRG_577t1:c.812T>C	NP_000479.1:p.Phe271Ser
XM_005245198.2:c.668T>C	XP_005245255.1:p.Phe223Ser
NM_001365052.1:c.668T>C	NP_001351981.1:p.Phe223Ser
NM_000488.4:c.812T>C MANE Select	NP_000479.1:p.Phe271Ser
NM_001365052.2:c.668T>C	NP_001351981.1:p.Phe223Ser
NM_001386302.1:c.935T>C	NP_001373231.1:p.Phe312Ser
NM_001386303.1:c.893T>C	NP_001373232.1:p.Phe298Ser
NM_001386304.1:c.791T>C	NP_001373233.1:p.Phe264Ser
NM_001386305.1:c.763-8T>C	NP_001373234.1:n.763-8T>C
NM_001386306.1:c.596T>C	NP_001373235.1:p.Phe199Ser