Canonical Allele Identifier: CA2692655245
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687074_136687078dup , CM000671.2:g.136687074_136687078dup GRCh38
NC_000009.11:g.139581526_139581530dup , CM000671.1:g.139581526_139581530dup GRCh37
NC_000009.10:g.138701347_138701351dup NCBI36
NG_008090.1:g.5387_5391dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.182+103_182+107dup MANE Select ENSP00000360761.2:n.182+103_182+107dup
ENST00000371694.7:c.182+103_182+107dup ENSP00000360759.3:n.182+103_182+107dup
ENST00000371696.6:c.182+103_182+107dup ENSP00000360761.2:n.182+103_182+107dup
ENST00000470861.1:n.190+103_190+107dup
ENST00000538402.1:c.182+103_182+107dup ENSP00000438919.1:n.182+103_182+107dup
NM_001012727.1:c.182+103_182+107dup NP_001012745.1:n.182+103_182+107dup
NM_006412.3:c.182+103_182+107dup NP_006403.2:n.182+103_182+107dup
NM_006412.4:c.182+103_182+107dup MANE Select NP_006403.2:n.182+103_182+107dup
NM_001012727.2:c.182+103_182+107dup NP_001012745.1:n.182+103_182+107dup