Canonical Allele Identifier: CA343772393

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173903973-G-T
• MyVariant Identifiers: chr1:g.173873111G>T (hg19) ; chr1:g.173903973G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903973G>T , CM000663.2:g.173903973G>T	GRCh38
NC_000001.10:g.173873111G>T , CM000663.1:g.173873111G>T	GRCh37
NC_000001.9:g.172139734G>T	NCBI36
NG_012462.1:g.18406C>A , LRG_577:g.18406C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1311C>A MANE Select	ENSP00000356671.3:p.Asn437Lys
ENST00000367698.3:c.1311C>A	ENSP00000356671.3:p.Asn437Lys
ENST00000617423.4:c.696C>A	ENSP00000478688.1:p.Asn232Lys
NM_000488.3:c.1311C>A , LRG_577t1:c.1311C>A	NP_000479.1:p.Asn437Lys
XM_005245198.2:c.1167C>A	XP_005245255.1:p.Asn389Lys
NM_001365052.1:c.1167C>A	NP_001351981.1:p.Asn389Lys
NM_000488.4:c.1311C>A MANE Select	NP_000479.1:p.Asn437Lys
NM_001365052.2:c.1167C>A	NP_001351981.1:p.Asn389Lys
NM_001386302.1:c.1434C>A	NP_001373231.1:p.Asn478Lys
NM_001386303.1:c.1392C>A	NP_001373232.1:p.Asn464Lys
NM_001386304.1:c.1290C>A	NP_001373233.1:p.Asn430Lys
NM_001386305.1:c.1254C>A	NP_001373234.1:p.Asn418Lys
NM_001386306.1:c.1095C>A	NP_001373235.1:p.Asn365Lys