Canonical Allele Identifier: CA1677440725

Gene: AGPAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161254459T= , CM000668.2:g.161254459T=	GRCh38
NC_000006.11:g.161675491T= , CM000668.1:g.161675491T=	GRCh37
NC_000006.10:g.161595481T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020133.3:c.-90+19479A= MANE Select	NP_064518.1:n.-90+19479A=
ENST00000320285.9:c.-90+19479A= MANE Select	ENSP00000314036.4:n.-90+19479A=
NM_020133.2:c.-90+19479A=	NP_064518.1:n.-90+19479A=
ENST00000320285.8:c.-90+19479A=	ENSP00000314036.4:n.-90+19479A=
ENST00000366905.3:c.-90+19479A=	ENSP00000355872.3:n.-90+19479A=
ENST00000366911.9:c.-90+19479A=	ENSP00000355878.5:n.-90+19479A=
ENST00000624499.2:n.26+19479A=
XM_005267053.2:c.-322+19479A=	XP_005267110.1:n.-322+19479A=
XM_005267053.3:c.-322+19479A=	XP_005267110.1:n.-322+19479A=
XM_006715512.2:c.-90+19359A=	XP_006715575.1:n.-90+19359A=
XM_006715514.2:c.-90+19479A=	XP_006715577.1:n.-90+19479A=
XM_006715514.3:c.-90+19479A=	XP_006715577.1:n.-90+19479A=
XM_006715515.2:c.-90+19479A=	XP_006715578.1:n.-90+19479A=
XM_017011059.1:c.-629+19479A=	XP_016866548.1:n.-629+19479A=
XR_001743516.1:n.124+19479A=