Canonical Allele Identifier: CA2739292067

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909603del , CM000663.2:g.173909603del	GRCh38
NC_000001.10:g.173878741del , CM000663.1:g.173878741del	GRCh37
NC_000001.9:g.172145364del	NCBI36
NG_012462.1:g.12776del , LRG_577:g.12776del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1102del MANE Select	ENSP00000356671.3:p.Gln368LysfsTer?
ENST00000367698.3:c.1102del	ENSP00000356671.3:p.Gln368LysfsTer?
ENST00000617423.4:c.560-2110del	ENSP00000478688.1:n.560-2110del
NM_000488.3:c.1102del , LRG_577t1:c.1102del	NP_000479.1:p.Gln368LysfsTer?
XM_005245198.2:c.958del	XP_005245255.1:p.Gln320LysfsTer?
NM_001365052.1:c.958del	NP_001351981.1:p.Gln320LysfsTer?
NM_000488.4:c.1102del MANE Select	NP_000479.1:p.Gln368LysfsTer?
NM_001365052.2:c.958del	NP_001351981.1:p.Gln320LysfsTer?
NM_001386302.1:c.1225del	NP_001373231.1:p.Gln409LysfsTer?
NM_001386303.1:c.1183del	NP_001373232.1:p.Gln395LysfsTer?
NM_001386304.1:c.1081del	NP_001373233.1:p.Gln361LysfsTer?
NM_001386305.1:c.1045del	NP_001373234.1:p.Gln349LysfsTer?
NM_001386306.1:c.886del	NP_001373235.1:p.Gln296LysfsTer?