Canonical Allele Identifier: CA343773969

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878855C>G (hg19) ; chr1:g.173909717C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909717C>G , CM000663.2:g.173909717C>G	GRCh38
NC_000001.10:g.173878855C>G , CM000663.1:g.173878855C>G	GRCh37
NC_000001.9:g.172145478C>G	NCBI36
NG_012462.1:g.12662G>C , LRG_577:g.12662G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.988G>C MANE Select	ENSP00000356671.3:p.Glu330Gln
ENST00000367698.3:c.988G>C	ENSP00000356671.3:p.Glu330Gln
ENST00000617423.4:c.559+2147G>C	ENSP00000478688.1:n.559+2147G>C
NM_000488.3:c.988G>C , LRG_577t1:c.988G>C	NP_000479.1:p.Glu330Gln
XM_005245198.2:c.844G>C	XP_005245255.1:p.Glu282Gln
NM_001365052.1:c.844G>C	NP_001351981.1:p.Glu282Gln
NM_000488.4:c.988G>C MANE Select	NP_000479.1:p.Glu330Gln
NM_001365052.2:c.844G>C	NP_001351981.1:p.Glu282Gln
NM_001386302.1:c.1111G>C	NP_001373231.1:p.Glu371Gln
NM_001386303.1:c.1069G>C	NP_001373232.1:p.Glu357Gln
NM_001386304.1:c.967G>C	NP_001373233.1:p.Glu323Gln
NM_001386305.1:c.931G>C	NP_001373234.1:p.Glu311Gln
NM_001386306.1:c.772G>C	NP_001373235.1:p.Glu258Gln