Canonical Allele Identifier: CA2838523848

Gene: ZGPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63712617T>C , CM000682.2:g.63712617T>C	GRCh38
NC_000020.10:g.62343969T>C , CM000682.1:g.62343969T>C	GRCh37
NC_000020.9:g.61814413T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355969.11:c.584+3453T>C MANE Select	ENSP00000348242.6:n.584+3453T>C
ENST00000328969.5:c.584+3453T>C	ENSP00000332013.5:n.584+3453T>C
ENST00000355969.10:c.584+3453T>C	ENSP00000348242.6:n.584+3453T>C
ENST00000357119.8:c.584+3453T>C	ENSP00000349634.4:n.584+3453T>C
ENST00000369967.7:c.584+3453T>C	ENSP00000358984.3:n.584+3453T>C
ENST00000448100.6:c.584+3453T>C	ENSP00000391176.1:n.584+3453T>C
ENST00000468235.1:n.76+3453T>C
ENST00000472711.5:n.284+3453T>C
ENST00000477340.5:n.692+3453T>C
ENST00000478385.5:n.167+3453T>C
ENST00000490623.3:c.301+3453T>C
NM_001083113.1:c.584+3453T>C	NP_001076582.1:n.584+3453T>C
NM_001195653.1:c.584+3453T>C	NP_001182582.1:n.584+3453T>C
NM_001195654.1:c.584+3453T>C	NP_001182583.1:n.584+3453T>C
NM_032527.4:c.584+3453T>C	NP_115916.3:n.584+3453T>C
NM_181485.2:c.584+3453T>C	NP_852150.2:n.584+3453T>C
NM_001083113.2:c.584+3453T>C	NP_001076582.1:n.584+3453T>C
NM_001195653.2:c.584+3453T>C	NP_001182582.1:n.584+3453T>C
NM_001195654.2:c.584+3453T>C	NP_001182583.1:n.584+3453T>C
NM_032527.5:c.584+3453T>C	NP_115916.3:n.584+3453T>C
NM_181485.3:c.584+3453T>C MANE Select	NP_852150.2:n.584+3453T>C