Canonical Allele Identifier: CA343774384

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878956G>T (hg19) ; chr1:g.173909818G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909818G>T , CM000663.2:g.173909818G>T	GRCh38
NC_000001.10:g.173878956G>T , CM000663.1:g.173878956G>T	GRCh37
NC_000001.9:g.172145579G>T	NCBI36
NG_012462.1:g.12561C>A , LRG_577:g.12561C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.887C>A MANE Select	ENSP00000356671.3:p.Ala296Asp
ENST00000367698.3:c.887C>A	ENSP00000356671.3:p.Ala296Asp
ENST00000487183.1:n.538C>A
ENST00000617423.4:c.559+2046C>A	ENSP00000478688.1:n.559+2046C>A
NM_000488.3:c.887C>A , LRG_577t1:c.887C>A	NP_000479.1:p.Ala296Asp
XM_005245198.2:c.743C>A	XP_005245255.1:p.Ala248Asp
NM_001365052.1:c.743C>A	NP_001351981.1:p.Ala248Asp
NM_000488.4:c.887C>A MANE Select	NP_000479.1:p.Ala296Asp
NM_001365052.2:c.743C>A	NP_001351981.1:p.Ala248Asp
NM_001386302.1:c.1010C>A	NP_001373231.1:p.Ala337Asp
NM_001386303.1:c.968C>A	NP_001373232.1:p.Ala323Asp
NM_001386304.1:c.866C>A	NP_001373233.1:p.Ala289Asp
NM_001386305.1:c.830C>A	NP_001373234.1:p.Ala277Asp
NM_001386306.1:c.671C>A	NP_001373235.1:p.Ala224Asp