Canonical Allele Identifier: CA2692654074

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674636-ACG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674637_136674638del , CM000671.2:g.136674637_136674638del	GRCh38
NC_000009.11:g.139569089_139569090del , CM000671.1:g.139569089_139569090del	GRCh37
NC_000009.10:g.138688910_138688911del	NCBI36
NG_008090.1:g.17822_17823del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.661+97_661+98del MANE Select	ENSP00000360761.2:n.661+97_661+98del
ENST00000371694.7:c.565+97_565+98del	ENSP00000360759.3:n.565+97_565+98del
ENST00000371696.6:c.661+97_661+98del	ENSP00000360761.2:n.661+97_661+98del
ENST00000472820.1:n.589+97_589+98del
ENST00000538402.1:c.661+97_661+98del	ENSP00000438919.1:n.661+97_661+98del
NM_001012727.1:c.565+97_565+98del	NP_001012745.1:n.565+97_565+98del
NM_006412.3:c.661+97_661+98del	NP_006403.2:n.661+97_661+98del
NM_006412.4:c.661+97_661+98del MANE Select	NP_006403.2:n.661+97_661+98del
NM_001012727.2:c.565+97_565+98del	NP_001012745.1:n.565+97_565+98del