Canonical Allele Identifier: CA421821504

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173903979-C-T
• MyVariant Identifiers: chr1:g.173873117C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903979C>T , CM000663.2:g.173903979C>T	GRCh38
NC_000001.10:g.173873117C>T , CM000663.1:g.173873117C>T	GRCh37
NC_000001.9:g.172139740C>T	NCBI36
NG_012462.1:g.18400G>A , LRG_577:g.18400G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1305G>A MANE Select	ENSP00000356671.3:p.Lys435=
ENST00000367698.3:c.1305G>A	ENSP00000356671.3:p.Lys435=
ENST00000617423.4:c.690G>A	ENSP00000478688.1:p.Lys230=
NM_000488.3:c.1305G>A , LRG_577t1:c.1305G>A	NP_000479.1:p.Lys435=
XM_005245198.2:c.1161G>A	XP_005245255.1:p.Lys387=
NM_001365052.1:c.1161G>A	NP_001351981.1:p.Lys387=
NM_000488.4:c.1305G>A MANE Select	NP_000479.1:p.Lys435=
NM_001365052.2:c.1161G>A	NP_001351981.1:p.Lys387=
NM_001386302.1:c.1428G>A	NP_001373231.1:p.Lys476=
NM_001386303.1:c.1386G>A	NP_001373232.1:p.Lys462=
NM_001386304.1:c.1284G>A	NP_001373233.1:p.Lys428=
NM_001386305.1:c.1248G>A	NP_001373234.1:p.Lys416=
NM_001386306.1:c.1089G>A	NP_001373235.1:p.Lys363=