Canonical Allele Identifier: CA2692654111

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674658-A-ACCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674658_136674659insCCG , CM000671.2:g.136674658_136674659insCCG	GRCh38
NC_000009.11:g.139569110_139569111insCCG , CM000671.1:g.139569110_139569111insCCG	GRCh37
NC_000009.10:g.138688931_138688932insCCG	NCBI36
NG_008090.1:g.17801_17802insCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.661+76_661+77insCGG MANE Select	ENSP00000360761.2:n.661+76_661+77insCGG
ENST00000371694.7:c.565+76_565+77insCGG	ENSP00000360759.3:n.565+76_565+77insCGG
ENST00000371696.6:c.661+76_661+77insCGG	ENSP00000360761.2:n.661+76_661+77insCGG
ENST00000472820.1:n.589+76_589+77insCGG
ENST00000538402.1:c.661+76_661+77insCGG	ENSP00000438919.1:n.661+76_661+77insCGG
NM_001012727.1:c.565+76_565+77insCGG	NP_001012745.1:n.565+76_565+77insCGG
NM_006412.3:c.661+76_661+77insCGG	NP_006403.2:n.661+76_661+77insCGG
NM_006412.4:c.661+76_661+77insCGG MANE Select	NP_006403.2:n.661+76_661+77insCGG
NM_001012727.2:c.565+76_565+77insCGG	NP_001012745.1:n.565+76_565+77insCGG