Canonical Allele Identifier: CA201627704

Gene: AGPAT2

Linked Data

• dbSNP Id: rs752290440
• MyVariant Identifiers: chr9:g.139569271_139569272insC (hg19) ; chr9:g.136674819_136674820insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674819_136674820insC , CM000671.2:g.136674819_136674820insC	GRCh38
NC_000009.11:g.139569271_139569272insC , CM000671.1:g.139569271_139569272insC	GRCh37
NC_000009.10:g.138689092_138689093insC	NCBI36
NG_008090.1:g.17640_17641insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.589-13_589-12insG MANE Select	ENSP00000360761.2:n.589-13_589-12insG
ENST00000371694.7:c.493-13_493-12insG	ENSP00000360759.3:n.493-13_493-12insG
ENST00000371696.6:c.589-13_589-12insG	ENSP00000360761.2:n.589-13_589-12insG
ENST00000472820.1:n.517-13_517-12insG
ENST00000538402.1:c.589-13_589-12insG	ENSP00000438919.1:n.589-13_589-12insG
NM_001012727.1:c.493-13_493-12insG	NP_001012745.1:n.493-13_493-12insG
NM_006412.3:c.589-13_589-12insG	NP_006403.2:n.589-13_589-12insG
NM_006412.4:c.589-13_589-12insG MANE Select	NP_006403.2:n.589-13_589-12insG
NM_001012727.2:c.493-13_493-12insG	NP_001012745.1:n.493-13_493-12insG