Canonical Allele Identifier: CA2374946261

Gene: ZGPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63712104_63712106delinsCTA , CM000682.2:g.63712104_63712106delinsCTA	GRCh38
NC_000020.10:g.62343456_62343458delinsCTA , CM000682.1:g.62343456_62343458delinsCTA	GRCh37
NC_000020.9:g.61813900_61813902delinsCTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355969.11:c.584+2940_584+2942delinsCTA MANE Select	ENSP00000348242.6:n.584+2940_584+2942delinsCTA
ENST00000328969.5:c.584+2940_584+2942delinsCTA	ENSP00000332013.5:n.584+2940_584+2942delinsCTA
ENST00000355969.10:c.584+2940_584+2942delinsCTA	ENSP00000348242.6:n.584+2940_584+2942delinsCTA
ENST00000357119.8:c.584+2940_584+2942delinsCTA	ENSP00000349634.4:n.584+2940_584+2942delinsCTA
ENST00000369967.7:c.584+2940_584+2942delinsCTA	ENSP00000358984.3:n.584+2940_584+2942delinsCTA
ENST00000448100.6:c.584+2940_584+2942delinsCTA	ENSP00000391176.1:n.584+2940_584+2942delinsCTA
ENST00000468235.1:n.76+2940_76+2942delinsCTA
ENST00000472711.5:n.284+2940_284+2942delinsCTA
ENST00000477340.5:n.692+2940_692+2942delinsCTA
ENST00000478385.5:n.167+2940_167+2942delinsCTA
ENST00000490623.3:c.301+2940_301+2942delinsCTA
NM_001083113.1:c.584+2940_584+2942delinsCTA	NP_001076582.1:n.584+2940_584+2942delinsCTA
NM_001195653.1:c.584+2940_584+2942delinsCTA	NP_001182582.1:n.584+2940_584+2942delinsCTA
NM_001195654.1:c.584+2940_584+2942delinsCTA	NP_001182583.1:n.584+2940_584+2942delinsCTA
NM_032527.4:c.584+2940_584+2942delinsCTA	NP_115916.3:n.584+2940_584+2942delinsCTA
NM_181485.2:c.584+2940_584+2942delinsCTA	NP_852150.2:n.584+2940_584+2942delinsCTA
NM_001083113.2:c.584+2940_584+2942delinsCTA	NP_001076582.1:n.584+2940_584+2942delinsCTA
NM_001195653.2:c.584+2940_584+2942delinsCTA	NP_001182582.1:n.584+2940_584+2942delinsCTA
NM_001195654.2:c.584+2940_584+2942delinsCTA	NP_001182583.1:n.584+2940_584+2942delinsCTA
NM_032527.5:c.584+2940_584+2942delinsCTA	NP_115916.3:n.584+2940_584+2942delinsCTA
NM_181485.3:c.584+2940_584+2942delinsCTA MANE Select	NP_852150.2:n.584+2940_584+2942delinsCTA