Canonical Allele Identifier: CA343773747

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878804T>C (hg19) ; chr1:g.173909666T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909666T>C , CM000663.2:g.173909666T>C	GRCh38
NC_000001.10:g.173878804T>C , CM000663.1:g.173878804T>C	GRCh37
NC_000001.9:g.172145427T>C	NCBI36
NG_012462.1:g.12713A>G , LRG_577:g.12713A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1039A>G MANE Select	ENSP00000356671.3:p.Met347Val
ENST00000367698.3:c.1039A>G	ENSP00000356671.3:p.Met347Val
ENST00000617423.4:c.560-2173A>G	ENSP00000478688.1:n.560-2173A>G
NM_000488.3:c.1039A>G , LRG_577t1:c.1039A>G	NP_000479.1:p.Met347Val
XM_005245198.2:c.895A>G	XP_005245255.1:p.Met299Val
NM_001365052.1:c.895A>G	NP_001351981.1:p.Met299Val
NM_000488.4:c.1039A>G MANE Select	NP_000479.1:p.Met347Val
NM_001365052.2:c.895A>G	NP_001351981.1:p.Met299Val
NM_001386302.1:c.1162A>G	NP_001373231.1:p.Met388Val
NM_001386303.1:c.1120A>G	NP_001373232.1:p.Met374Val
NM_001386304.1:c.1018A>G	NP_001373233.1:p.Met340Val
NM_001386305.1:c.982A>G	NP_001373234.1:p.Met328Val
NM_001386306.1:c.823A>G	NP_001373235.1:p.Met275Val