Canonical Allele Identifier: CA2500999776

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676907-TGGCCCCGCCCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676914_136676924del , CM000671.2:g.136676914_136676924del	GRCh38
NC_000009.11:g.139571366_139571376del , CM000671.1:g.139571366_139571376del	GRCh37
NC_000009.10:g.138691187_138691197del	NCBI36
NG_008090.1:g.15542_15552del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+43_492+53del MANE Select	ENSP00000360761.2:n.492+43_492+53del
ENST00000371694.7:c.492+43_492+53del	ENSP00000360759.3:n.492+43_492+53del
ENST00000371696.6:c.492+43_492+53del	ENSP00000360761.2:n.492+43_492+53del
ENST00000472820.1:n.420+43_420+53del
ENST00000538402.1:c.492+43_492+53del	ENSP00000438919.1:n.492+43_492+53del
NM_001012727.1:c.492+43_492+53del	NP_001012745.1:n.492+43_492+53del
NM_006412.3:c.492+43_492+53del	NP_006403.2:n.492+43_492+53del
NM_006412.4:c.492+43_492+53del MANE Select	NP_006403.2:n.492+43_492+53del
NM_001012727.2:c.492+43_492+53del	NP_001012745.1:n.492+43_492+53del