Canonical Allele Identifier: CA2786279782
Gene: AGPAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674676G>C , CM000671.2:g.136674676G>C GRCh38
NC_000009.11:g.139569128G>C , CM000671.1:g.139569128G>C GRCh37
NC_000009.10:g.138688949G>C NCBI36
NG_008090.1:g.17784C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.661+59C>G MANE Select ENSP00000360761.2:n.661+59C>G
ENST00000371694.7:c.565+59C>G ENSP00000360759.3:n.565+59C>G
ENST00000371696.6:c.661+59C>G ENSP00000360761.2:n.661+59C>G
ENST00000472820.1:n.589+59C>G
ENST00000538402.1:c.661+59C>G ENSP00000438919.1:n.661+59C>G
NM_001012727.1:c.565+59C>G NP_001012745.1:n.565+59C>G
NM_006412.3:c.661+59C>G NP_006403.2:n.661+59C>G
NM_006412.4:c.661+59C>G MANE Select NP_006403.2:n.661+59C>G
NM_001012727.2:c.565+59C>G NP_001012745.1:n.565+59C>G
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