Canonical Allele Identifier: CA2692655375
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687306_136687317dup , CM000671.2:g.136687306_136687317dup GRCh38
NC_000009.11:g.139581758_139581769dup , CM000671.1:g.139581758_139581769dup GRCh37
NC_000009.10:g.138701579_138701590dup NCBI36
NG_008090.1:g.5146_5157dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.44_55dup MANE Select ENSP00000360761.2:p.Val18_Gln19insLeuLeuLeuVal
ENST00000371694.7:c.44_55dup ENSP00000360759.3:p.Val18_Gln19insLeuLeuLeuVal
ENST00000371696.6:c.44_55dup ENSP00000360761.2:p.Val18_Gln19insLeuLeuLeuVal
ENST00000470861.1:n.52_63dup
ENST00000538402.1:c.44_55dup ENSP00000438919.1:p.Val18_Gln19insLeuLeuLeuVal
NM_001012727.1:c.44_55dup NP_001012745.1:p.Val18_Gln19insLeuLeuLeuVal
NM_006412.3:c.44_55dup NP_006403.2:p.Val18_Gln19insLeuLeuLeuVal
NM_006412.4:c.44_55dup MANE Select NP_006403.2:p.Val18_Gln19insLeuLeuLeuVal
NM_001012727.2:c.44_55dup NP_001012745.1:p.Val18_Gln19insLeuLeuLeuVal