Canonical Allele Identifier: CA343773562

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909599T>C , CM000663.2:g.173909599T>C	GRCh38
NC_000001.10:g.173878737T>C , CM000663.1:g.173878737T>C	GRCh37
NC_000001.9:g.172145360T>C	NCBI36
NG_012462.1:g.12780A>G , LRG_577:g.12780A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000488.4:c.1106A>G MANE Select	NP_000479.1:p.Asp369Gly
ENST00000367698.4:c.1106A>G MANE Select	ENSP00000356671.3:p.Asp369Gly
NM_000488.3:c.1106A>G , LRG_577t1:c.1106A>G	NP_000479.1:p.Asp369Gly
NM_001365052.1:c.962A>G	NP_001351981.1:p.Asp321Gly
NM_001365052.2:c.962A>G	NP_001351981.1:p.Asp321Gly
NM_001386302.1:c.1229A>G	NP_001373231.1:p.Asp410Gly
NM_001386303.1:c.1187A>G	NP_001373232.1:p.Asp396Gly
NM_001386304.1:c.1085A>G	NP_001373233.1:p.Asp362Gly
NM_001386305.1:c.1049A>G	NP_001373234.1:p.Asp350Gly
NM_001386306.1:c.890A>G	NP_001373235.1:p.Asp297Gly
ENST00000367698.3:c.1106A>G	ENSP00000356671.3:p.Asp369Gly
ENST00000617423.4:c.560-2106A>G	ENSP00000478688.1:n.560-2106A>G
XM_005245198.2:c.962A>G	XP_005245255.1:p.Asp321Gly