Canonical Allele Identifier: CA1207937242

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173910374_173910377delinsCAAG , CM000663.2:g.173910374_173910377delinsCAAG	GRCh38
NC_000001.10:g.173879512_173879515delinsCAAG , CM000663.1:g.173879512_173879515delinsCAAG	GRCh37
NC_000001.9:g.172146135_172146138delinsCAAG	NCBI36
NG_012462.1:g.12002_12005delinsCTTG , LRG_577:g.12002_12005delinsCTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.762+377_762+380delinsCTTG MANE Select	ENSP00000356671.3:n.762+377_762+380delins...
ENST00000367698.3:c.762+377_762+380delinsCTTG	ENSP00000356671.3:n.762+377_762+380delins...
ENST00000487183.1:n.413+377_413+380delinsCTTG
ENST00000617423.4:c.559+1487_559+1490delinsCTTG	ENSP00000478688.1:n.559+1487_559+1490deli...
NM_000488.3:c.762+377_762+380delinsCTTG , LRG_577t1:c.762+377_762+380delinsCTTG	NP_000479.1:n.762+377_762+380delinsCTTG
XM_005245198.2:c.618+377_618+380delinsCTTG	XP_005245255.1:n.618+377_618+380delinsCTT...
NM_001365052.1:c.618+377_618+380delinsCTTG	NP_001351981.1:n.618+377_618+380delinsCTT...
NM_000488.4:c.762+377_762+380delinsCTTG MANE Select	NP_000479.1:n.762+377_762+380delinsCTTG
NM_001365052.2:c.618+377_618+380delinsCTTG	NP_001351981.1:n.618+377_618+380delinsCTT...
NM_001386302.1:c.885+254_885+257delinsCTTG	NP_001373231.1:n.885+254_885+257delinsCTT...
NM_001386303.1:c.843+377_843+380delinsCTTG	NP_001373232.1:n.843+377_843+380delinsCTT...
NM_001386304.1:c.741+398_741+401delinsCTTG	NP_001373233.1:n.741+398_741+401delinsCTT...
NM_001386305.1:c.762+377_762+380delinsCTTG	NP_001373234.1:n.762+377_762+380delinsCTT...
NM_001386306.1:c.546+377_546+380delinsCTTG	NP_001373235.1:n.546+377_546+380delinsCTT...