Canonical Allele Identifier: CA2692653767
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673870_136673887dup , CM000671.2:g.136673870_136673887dup GRCh38
NC_000009.11:g.139568322_139568339dup , CM000671.1:g.139568322_139568339dup GRCh37
NC_000009.10:g.138688143_138688160dup NCBI36
NG_008090.1:g.18575_18592dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.704_721dup MANE Select ENSP00000360761.2:p.Asp240_Val241insGlyLeuThrAlaAlaAsp
ENST00000371694.7:c.608_625dup ENSP00000360759.3:p.Asp208_Val209insGlyLeuThrAlaAlaAsp
ENST00000371696.6:c.704_721dup ENSP00000360761.2:p.Asp240_Val241insGlyLeuThrAlaAlaAsp
ENST00000472820.1:n.632_649dup
ENST00000538402.1:c.704_721dup ENSP00000438919.1:p.Asp240_Val241insGlyLeuThrAlaAlaAsp
NM_001012727.1:c.608_625dup NP_001012745.1:p.Asp208_Val209insGlyLeuThrAlaAlaAsp
NM_006412.3:c.704_721dup NP_006403.2:p.Asp240_Val241insGlyLeuThrAlaAlaAsp
NM_006412.4:c.704_721dup MANE Select NP_006403.2:p.Asp240_Val241insGlyLeuThrAlaAlaAsp
NM_001012727.2:c.608_625dup NP_001012745.1:p.Asp208_Val209insGlyLeuThrAlaAlaAsp