Canonical Allele Identifier: CA343774195

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878910G>C (hg19) ; chr1:g.173909772G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909772G>C , CM000663.2:g.173909772G>C	GRCh38
NC_000001.10:g.173878910G>C , CM000663.1:g.173878910G>C	GRCh37
NC_000001.9:g.172145533G>C	NCBI36
NG_012462.1:g.12607C>G , LRG_577:g.12607C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.933C>G MANE Select	ENSP00000356671.3:p.Ile311Met
ENST00000367698.3:c.933C>G	ENSP00000356671.3:p.Ile311Met
ENST00000487183.1:n.584C>G
ENST00000617423.4:c.559+2092C>G	ENSP00000478688.1:n.559+2092C>G
NM_000488.3:c.933C>G , LRG_577t1:c.933C>G	NP_000479.1:p.Ile311Met
XM_005245198.2:c.789C>G	XP_005245255.1:p.Ile263Met
NM_001365052.1:c.789C>G	NP_001351981.1:p.Ile263Met
NM_000488.4:c.933C>G MANE Select	NP_000479.1:p.Ile311Met
NM_001365052.2:c.789C>G	NP_001351981.1:p.Ile263Met
NM_001386302.1:c.1056C>G	NP_001373231.1:p.Ile352Met
NM_001386303.1:c.1014C>G	NP_001373232.1:p.Ile338Met
NM_001386304.1:c.912C>G	NP_001373233.1:p.Ile304Met
NM_001386305.1:c.876C>G	NP_001373234.1:p.Ile292Met
NM_001386306.1:c.717C>G	NP_001373235.1:p.Ile239Met