Canonical Allele Identifier: CA343774422

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878967A>T (hg19) ; chr1:g.173909829A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909829A>T , CM000663.2:g.173909829A>T	GRCh38
NC_000001.10:g.173878967A>T , CM000663.1:g.173878967A>T	GRCh37
NC_000001.9:g.172145590A>T	NCBI36
NG_012462.1:g.12550T>A , LRG_577:g.12550T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.876T>A MANE Select	ENSP00000356671.3:p.Tyr292Ter
ENST00000367698.3:c.876T>A	ENSP00000356671.3:p.Tyr292Ter
ENST00000487183.1:n.527T>A
ENST00000617423.4:c.559+2035T>A	ENSP00000478688.1:n.559+2035T>A
NM_000488.3:c.876T>A , LRG_577t1:c.876T>A	NP_000479.1:p.Tyr292Ter
XM_005245198.2:c.732T>A	XP_005245255.1:p.Tyr244Ter
NM_001365052.1:c.732T>A	NP_001351981.1:p.Tyr244Ter
NM_000488.4:c.876T>A MANE Select	NP_000479.1:p.Tyr292Ter
NM_001365052.2:c.732T>A	NP_001351981.1:p.Tyr244Ter
NM_001386302.1:c.999T>A	NP_001373231.1:p.Tyr333Ter
NM_001386303.1:c.957T>A	NP_001373232.1:p.Tyr319Ter
NM_001386304.1:c.855T>A	NP_001373233.1:p.Tyr285Ter
NM_001386305.1:c.819T>A	NP_001373234.1:p.Tyr273Ter
NM_001386306.1:c.660T>A	NP_001373235.1:p.Tyr220Ter