Canonical Allele Identifier: CA746510745

Gene: ZGPAT

Linked Data

• dbSNP Id: rs1397228582
• MyVariant Identifiers: chr20:g.62343457_62343458del (hg19) ; chr20:g.63712105_63712106del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63712106_63712107del , CM000682.2:g.63712106_63712107del	GRCh38
NC_000020.10:g.62343458_62343459del , CM000682.1:g.62343458_62343459del	GRCh37
NC_000020.9:g.61813902_61813903del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355969.11:c.584+2942_584+2943del MANE Select	ENSP00000348242.6:n.584+2942_584+2943del
ENST00000328969.5:c.584+2942_584+2943del	ENSP00000332013.5:n.584+2942_584+2943del
ENST00000355969.10:c.584+2942_584+2943del	ENSP00000348242.6:n.584+2942_584+2943del
ENST00000357119.8:c.584+2942_584+2943del	ENSP00000349634.4:n.584+2942_584+2943del
ENST00000369967.7:c.584+2942_584+2943del	ENSP00000358984.3:n.584+2942_584+2943del
ENST00000448100.6:c.584+2942_584+2943del	ENSP00000391176.1:n.584+2942_584+2943del
ENST00000468235.1:n.76+2942_76+2943del
ENST00000472711.5:n.284+2942_284+2943del
ENST00000477340.5:n.692+2942_692+2943del
ENST00000478385.5:n.167+2942_167+2943del
ENST00000490623.3:c.301+2942_301+2943del
NM_001083113.1:c.584+2942_584+2943del	NP_001076582.1:n.584+2942_584+2943del
NM_001195653.1:c.584+2942_584+2943del	NP_001182582.1:n.584+2942_584+2943del
NM_001195654.1:c.584+2942_584+2943del	NP_001182583.1:n.584+2942_584+2943del
NM_032527.4:c.584+2942_584+2943del	NP_115916.3:n.584+2942_584+2943del
NM_181485.2:c.584+2942_584+2943del	NP_852150.2:n.584+2942_584+2943del
NM_001083113.2:c.584+2942_584+2943del	NP_001076582.1:n.584+2942_584+2943del
NM_001195653.2:c.584+2942_584+2943del	NP_001182582.1:n.584+2942_584+2943del
NM_001195654.2:c.584+2942_584+2943del	NP_001182583.1:n.584+2942_584+2943del
NM_032527.5:c.584+2942_584+2943del	NP_115916.3:n.584+2942_584+2943del
NM_181485.3:c.584+2942_584+2943del MANE Select	NP_852150.2:n.584+2942_584+2943del