Canonical Allele Identifier: CA421821220

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173903910-T-C
• MyVariant Identifiers: chr1:g.173873048T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903910T>C , CM000663.2:g.173903910T>C	GRCh38
NC_000001.10:g.173873048T>C , CM000663.1:g.173873048T>C	GRCh37
NC_000001.9:g.172139671T>C	NCBI36
NG_012462.1:g.18469A>G , LRG_577:g.18469A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1374A>G MANE Select	ENSP00000356671.3:p.Val458=
ENST00000367698.3:c.1374A>G	ENSP00000356671.3:p.Val458=
ENST00000617423.4:c.759A>G	ENSP00000478688.1:p.Val253=
NM_000488.3:c.1374A>G , LRG_577t1:c.1374A>G	NP_000479.1:p.Val458=
XM_005245198.2:c.1230A>G	XP_005245255.1:p.Val410=
NM_001365052.1:c.1230A>G	NP_001351981.1:p.Val410=
NM_000488.4:c.1374A>G MANE Select	NP_000479.1:p.Val458=
NM_001365052.2:c.1230A>G	NP_001351981.1:p.Val410=
NM_001386302.1:c.1497A>G	NP_001373231.1:p.Val499=
NM_001386303.1:c.1455A>G	NP_001373232.1:p.Val485=
NM_001386304.1:c.1353A>G	NP_001373233.1:p.Val451=
NM_001386305.1:c.1317A>G	NP_001373234.1:p.Val439=
NM_001386306.1:c.1158A>G	NP_001373235.1:p.Val386=