Canonical Allele Identifier: CA2692654345

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674885-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674885_136674886insT , CM000671.2:g.136674885_136674886insT	GRCh38
NC_000009.11:g.139569337_139569338insT , CM000671.1:g.139569337_139569338insT	GRCh37
NC_000009.10:g.138689158_138689159insT	NCBI36
NG_008090.1:g.17574_17575insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.589-79_589-78insA MANE Select	ENSP00000360761.2:n.589-79_589-78insA
ENST00000371694.7:c.493-79_493-78insA	ENSP00000360759.3:n.493-79_493-78insA
ENST00000371696.6:c.589-79_589-78insA	ENSP00000360761.2:n.589-79_589-78insA
ENST00000472820.1:n.517-79_517-78insA
ENST00000538402.1:c.589-79_589-78insA	ENSP00000438919.1:n.589-79_589-78insA
NM_001012727.1:c.493-79_493-78insA	NP_001012745.1:n.493-79_493-78insA
NM_006412.3:c.589-79_589-78insA	NP_006403.2:n.589-79_589-78insA
NM_006412.4:c.589-79_589-78insA MANE Select	NP_006403.2:n.589-79_589-78insA
NM_001012727.2:c.493-79_493-78insA	NP_001012745.1:n.493-79_493-78insA