Canonical Allele Identifier: CA2786279770

Gene: AGPAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674622_136674627del , CM000671.2:g.136674622_136674627del	GRCh38
NC_000009.11:g.139569074_139569079del , CM000671.1:g.139569074_139569079del	GRCh37
NC_000009.10:g.138688895_138688900del	NCBI36
NG_008090.1:g.17833_17838del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.661+108_661+113del MANE Select	ENSP00000360761.2:n.661+108_661+113del
ENST00000371694.7:c.565+108_565+113del	ENSP00000360759.3:n.565+108_565+113del
ENST00000371696.6:c.661+108_661+113del	ENSP00000360761.2:n.661+108_661+113del
ENST00000472820.1:n.589+108_589+113del
ENST00000538402.1:c.661+108_661+113del	ENSP00000438919.1:n.661+108_661+113del
NM_001012727.1:c.565+108_565+113del	NP_001012745.1:n.565+108_565+113del
NM_006412.3:c.661+108_661+113del	NP_006403.2:n.661+108_661+113del
NM_006412.4:c.661+108_661+113del MANE Select	NP_006403.2:n.661+108_661+113del
NM_001012727.2:c.565+108_565+113del	NP_001012745.1:n.565+108_565+113del