Canonical Allele Identifier: CA343773764

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878807T>C (hg19) ; chr1:g.173909669T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909669T>C , CM000663.2:g.173909669T>C	GRCh38
NC_000001.10:g.173878807T>C , CM000663.1:g.173878807T>C	GRCh37
NC_000001.9:g.172145430T>C	NCBI36
NG_012462.1:g.12710A>G , LRG_577:g.12710A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1036A>G MANE Select	ENSP00000356671.3:p.Met346Val
ENST00000367698.3:c.1036A>G	ENSP00000356671.3:p.Met346Val
ENST00000617423.4:c.560-2176A>G	ENSP00000478688.1:n.560-2176A>G
NM_000488.3:c.1036A>G , LRG_577t1:c.1036A>G	NP_000479.1:p.Met346Val
XM_005245198.2:c.892A>G	XP_005245255.1:p.Met298Val
NM_001365052.1:c.892A>G	NP_001351981.1:p.Met298Val
NM_000488.4:c.1036A>G MANE Select	NP_000479.1:p.Met346Val
NM_001365052.2:c.892A>G	NP_001351981.1:p.Met298Val
NM_001386302.1:c.1159A>G	NP_001373231.1:p.Met387Val
NM_001386303.1:c.1117A>G	NP_001373232.1:p.Met373Val
NM_001386304.1:c.1015A>G	NP_001373233.1:p.Met339Val
NM_001386305.1:c.979A>G	NP_001373234.1:p.Met327Val
NM_001386306.1:c.820A>G	NP_001373235.1:p.Met274Val