Canonical Allele Identifier: CA2786279629

Gene: AGPAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687045G>C , CM000671.2:g.136687045G>C	GRCh38
NC_000009.11:g.139581497G>C , CM000671.1:g.139581497G>C	GRCh37
NC_000009.10:g.138701318G>C	NCBI36
NG_008090.1:g.5415C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.182+131C>G MANE Select	ENSP00000360761.2:n.182+131C>G
ENST00000371694.7:c.182+131C>G	ENSP00000360759.3:n.182+131C>G
ENST00000371696.6:c.182+131C>G	ENSP00000360761.2:n.182+131C>G
ENST00000470861.1:n.190+131C>G
ENST00000538402.1:c.182+131C>G	ENSP00000438919.1:n.182+131C>G
NM_001012727.1:c.182+131C>G	NP_001012745.1:n.182+131C>G
NM_006412.3:c.182+131C>G	NP_006403.2:n.182+131C>G
NM_006412.4:c.182+131C>G MANE Select	NP_006403.2:n.182+131C>G
NM_001012727.2:c.182+131C>G	NP_001012745.1:n.182+131C>G