Canonical Allele Identifier: CA343772692

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873198A>T (hg19) ; chr1:g.173904060A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904060A>T , CM000663.2:g.173904060A>T	GRCh38
NC_000001.10:g.173873198A>T , CM000663.1:g.173873198A>T	GRCh37
NC_000001.9:g.172139821A>T	NCBI36
NG_012462.1:g.18319T>A , LRG_577:g.18319T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1224T>A MANE Select	ENSP00000356671.3:p.Asn408Lys
ENST00000367698.3:c.1224T>A	ENSP00000356671.3:p.Asn408Lys
ENST00000617423.4:c.609T>A	ENSP00000478688.1:p.Asn203Lys
NM_000488.3:c.1224T>A , LRG_577t1:c.1224T>A	NP_000479.1:p.Asn408Lys
XM_005245198.2:c.1080T>A	XP_005245255.1:p.Asn360Lys
NM_001365052.1:c.1080T>A	NP_001351981.1:p.Asn360Lys
NM_000488.4:c.1224T>A MANE Select	NP_000479.1:p.Asn408Lys
NM_001365052.2:c.1080T>A	NP_001351981.1:p.Asn360Lys
NM_001386302.1:c.1347T>A	NP_001373231.1:p.Asn449Lys
NM_001386303.1:c.1305T>A	NP_001373232.1:p.Asn435Lys
NM_001386304.1:c.1203T>A	NP_001373233.1:p.Asn401Lys
NM_001386305.1:c.1167T>A	NP_001373234.1:p.Asn389Lys
NM_001386306.1:c.1008T>A	NP_001373235.1:p.Asn336Lys