Canonical Allele Identifier: CA645547675

Gene: AGPAT2

Linked Data

• COSMIC: COSM4433938

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674790del , CM000671.2:g.136674790del	GRCh38
NC_000009.11:g.139569242del , CM000671.1:g.139569242del	GRCh37
NC_000009.10:g.138689063del	NCBI36
NG_008090.1:g.17671del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.607del MANE Select	ENSP00000360761.2:p.Val203CysfsTer?
ENST00000371694.7:c.511del	ENSP00000360759.3:p.Val171CysfsTer?
ENST00000371696.6:c.607del	ENSP00000360761.2:p.Val203CysfsTer?
ENST00000472820.1:n.535del
ENST00000538402.1:c.607del	ENSP00000438919.1:p.Val203CysfsTer?
NM_001012727.1:c.511del	NP_001012745.1:p.Val171CysfsTer?
NM_006412.3:c.607del	NP_006403.2:p.Val203CysfsTer?
NM_006412.4:c.607del MANE Select	NP_006403.2:p.Val203CysfsTer?
NM_001012727.2:c.511del	NP_001012745.1:p.Val171CysfsTer?