Canonical Allele Identifier: CA2786279702
Gene: AGPAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673847_136673868dup , CM000671.2:g.136673847_136673868dup GRCh38
NC_000009.11:g.139568299_139568320dup , CM000671.1:g.139568299_139568320dup GRCh37
NC_000009.10:g.138688120_138688141dup NCBI36
NG_008090.1:g.18593_18614dup

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.722_743dup MANE Select ENSP00000360761.2:p.His249ProfsTer?
ENST00000371694.7:c.626_647dup ENSP00000360759.3:p.His217ProfsTer?
ENST00000371696.6:c.722_743dup ENSP00000360761.2:p.His249ProfsTer?
ENST00000472820.1:n.650_671dup
ENST00000538402.1:c.722_743dup ENSP00000438919.1:p.His249ProfsTer?
NM_001012727.1:c.626_647dup NP_001012745.1:p.His217ProfsTer?
NM_006412.3:c.722_743dup NP_006403.2:p.His249ProfsTer?
NM_006412.4:c.722_743dup MANE Select NP_006403.2:p.His249ProfsTer?
NM_001012727.2:c.626_647dup NP_001012745.1:p.His217ProfsTer?