Canonical Allele Identifier: CA421821539

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873141T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904003T>A , CM000663.2:g.173904003T>A	GRCh38
NC_000001.10:g.173873141T>A , CM000663.1:g.173873141T>A	GRCh37
NC_000001.9:g.172139764T>A	NCBI36
NG_012462.1:g.18376A>T , LRG_577:g.18376A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1281A>T MANE Select	ENSP00000356671.3:p.Leu427=
ENST00000367698.3:c.1281A>T	ENSP00000356671.3:p.Leu427=
ENST00000617423.4:c.666A>T	ENSP00000478688.1:p.Leu222=
NM_000488.3:c.1281A>T , LRG_577t1:c.1281A>T	NP_000479.1:p.Leu427=
XM_005245198.2:c.1137A>T	XP_005245255.1:p.Leu379=
NM_001365052.1:c.1137A>T	NP_001351981.1:p.Leu379=
NM_000488.4:c.1281A>T MANE Select	NP_000479.1:p.Leu427=
NM_001365052.2:c.1137A>T	NP_001351981.1:p.Leu379=
NM_001386302.1:c.1404A>T	NP_001373231.1:p.Leu468=
NM_001386303.1:c.1362A>T	NP_001373232.1:p.Leu454=
NM_001386304.1:c.1260A>T	NP_001373233.1:p.Leu420=
NM_001386305.1:c.1224A>T	NP_001373234.1:p.Leu408=
NM_001386306.1:c.1065A>T	NP_001373235.1:p.Leu355=