Canonical Allele Identifier: CA343776312

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173880987C>T (hg19) ; chr1:g.173911849C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911849C>T , CM000663.2:g.173911849C>T	GRCh38
NC_000001.10:g.173880987C>T , CM000663.1:g.173880987C>T	GRCh37
NC_000001.9:g.172147610C>T	NCBI36
NG_012462.1:g.10530G>A , LRG_577:g.10530G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.574G>A MANE Select	ENSP00000356671.3:p.Asp192Asn
ENST00000367698.3:c.574G>A	ENSP00000356671.3:p.Asp192Asn
ENST00000487183.1:n.279G>A
ENST00000617423.4:c.559+15G>A	ENSP00000478688.1:n.559+15G>A
NM_000488.3:c.574G>A , LRG_577t1:c.574G>A	NP_000479.1:p.Asp192Asn
XM_005245198.2:c.430G>A	XP_005245255.1:p.Asp144Asn
NM_001365052.1:c.430G>A	NP_001351981.1:p.Asp144Asn
NM_000488.4:c.574G>A MANE Select	NP_000479.1:p.Asp192Asn
NM_001365052.2:c.430G>A	NP_001351981.1:p.Asp144Asn
NM_001386302.1:c.574G>A	NP_001373231.1:p.Asp192Asn
NM_001386303.1:c.655G>A	NP_001373232.1:p.Asp219Asn
NM_001386304.1:c.574G>A	NP_001373233.1:p.Asp192Asn
NM_001386305.1:c.574G>A	NP_001373234.1:p.Asp192Asn
NM_001386306.1:c.409-958G>A	NP_001373235.1:n.409-958G>A