Canonical Allele Identifier: CA2692654046

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674625-GTGGCCACGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674626_136674635del , CM000671.2:g.136674626_136674635del	GRCh38
NC_000009.11:g.139569078_139569087del , CM000671.1:g.139569078_139569087del	GRCh37
NC_000009.10:g.138688899_138688908del	NCBI36
NG_008090.1:g.17825_17834del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.661+100_661+109del MANE Select	ENSP00000360761.2:n.661+100_661+109del
ENST00000371694.7:c.565+100_565+109del	ENSP00000360759.3:n.565+100_565+109del
ENST00000371696.6:c.661+100_661+109del	ENSP00000360761.2:n.661+100_661+109del
ENST00000472820.1:n.589+100_589+109del
ENST00000538402.1:c.661+100_661+109del	ENSP00000438919.1:n.661+100_661+109del
NM_001012727.1:c.565+100_565+109del	NP_001012745.1:n.565+100_565+109del
NM_006412.3:c.661+100_661+109del	NP_006403.2:n.661+100_661+109del
NM_006412.4:c.661+100_661+109del MANE Select	NP_006403.2:n.661+100_661+109del
NM_001012727.2:c.565+100_565+109del	NP_001012745.1:n.565+100_565+109del