Canonical Allele Identifier: CA2786278287

Gene: AGPAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676917_136676918insCA , CM000671.2:g.136676917_136676918insCA	GRCh38
NC_000009.11:g.139571369_139571370insCA , CM000671.1:g.139571369_139571370insCA	GRCh37
NC_000009.10:g.138691190_138691191insCA	NCBI36
NG_008090.1:g.15542_15543insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+43_492+44insTG MANE Select	ENSP00000360761.2:n.492+43_492+44insTG
ENST00000371694.7:c.492+43_492+44insTG	ENSP00000360759.3:n.492+43_492+44insTG
ENST00000371696.6:c.492+43_492+44insTG	ENSP00000360761.2:n.492+43_492+44insTG
ENST00000472820.1:n.420+43_420+44insTG
ENST00000538402.1:c.492+43_492+44insTG	ENSP00000438919.1:n.492+43_492+44insTG
NM_001012727.1:c.492+43_492+44insTG	NP_001012745.1:n.492+43_492+44insTG
NM_006412.3:c.492+43_492+44insTG	NP_006403.2:n.492+43_492+44insTG
NM_006412.4:c.492+43_492+44insTG MANE Select	NP_006403.2:n.492+43_492+44insTG
NM_001012727.2:c.492+43_492+44insTG	NP_001012745.1:n.492+43_492+44insTG