Canonical Allele Identifier: CA4726820

Gene: GPAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41620928C>T , CM000670.2:g.41620928C>T	GRCh38
NC_000008.10:g.41478447C>T , CM000670.1:g.41478447C>T	GRCh37
NC_000008.9:g.41597604C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396987.7:c.1298C>T MANE Select	ENSP00000380184.3:p.Thr433Met
ENST00000518628.1:n.597C>T
ENST00000521349.1:n.397C>T
NM_178819.3:c.1298C>T	NP_848934.1:p.Thr433Met
XM_011544392.1:c.1298C>T	XP_011542694.1:p.Thr433Met
XM_011544393.1:c.1298C>T	XP_011542695.1:p.Thr433Met
XM_011544394.1:c.1298C>T	XP_011542696.1:p.Thr433Met
XM_011544396.1:c.1223C>T	XP_011542698.1:p.Thr408Met
XM_011544397.1:c.998C>T	XP_011542699.1:p.Thr333Met
NM_001363197.1:c.1298C>T	NP_001350126.1:p.Thr433Met
NM_001363198.1:c.674C>T	NP_001350127.1:p.Thr225Met
XR_001745474.1:n.2366C>T
NM_178819.4:c.1298C>T MANE Select	NP_848934.1:p.Thr433Met
NM_001363197.2:c.1298C>T	NP_001350126.1:p.Thr433Met
NM_001363198.2:c.674C>T	NP_001350127.1:p.Thr225Met