Canonical Allele Identifier: CA2786279609
Gene: AGPAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673625G>C , CM000671.2:g.136673625G>C GRCh38
NC_000009.11:g.139568077G>C , CM000671.1:g.139568077G>C GRCh37
NC_000009.10:g.138687898G>C NCBI36
NG_008090.1:g.18835C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*127C>G MANE Select ENSP00000360761.2:n.*127C>G
ENST00000371694.7:c.*127C>G ENSP00000360759.3:n.*127C>G
ENST00000371696.6:c.*127C>G ENSP00000360761.2:n.*127C>G
ENST00000538402.1:c.*127C>G ENSP00000438919.1:n.*127C>G
NM_001012727.1:c.*127C>G NP_001012745.1:n.*127C>G
NM_006412.3:c.*127C>G NP_006403.2:n.*127C>G
NM_006412.4:c.*127C>G MANE Select NP_006403.2:n.*127C>G
NM_001012727.2:c.*127C>G NP_001012745.1:n.*127C>G