Canonical Allele Identifier: CA2692654590
Community Standard Title: NM_006412.4(AGPAT2):c.538dup (p.Asp180GlyfsTer6)
Gene: AGPAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676638dup , CM000671.2:g.136676638dup GRCh38
NC_000009.11:g.139571090dup , CM000671.1:g.139571090dup GRCh37
NC_000009.10:g.138690911dup NCBI36
NG_008090.1:g.15825dup

Transcript Alleles

HGVS Amino-acid Change
NM_006412.4:c.538dup MANE Select NP_006403.2:p.Asp180GlyfsTer6
ENST00000371696.7:c.538dup MANE Select ENSP00000360761.2:p.Asp180GlyfsTer6
NM_001012727.1:c.492+326dup NP_001012745.1:n.492+326dup
NM_001012727.2:c.492+326dup NP_001012745.1:n.492+326dup
NM_006412.3:c.538dup NP_006403.2:p.Asp180GlyfsTer6
ENST00000371694.7:c.492+326dup ENSP00000360759.3:n.492+326dup
ENST00000371696.6:c.538dup ENSP00000360761.2:p.Asp180GlyfsTer6
ENST00000472820.1:n.466dup
ENST00000538402.1:c.538dup ENSP00000438919.1:p.Asp180GlyfsTer6