Canonical Allele Identifier: CA2692654194

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674712-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674712C>A , CM000671.2:g.136674712C>A	GRCh38
NC_000009.11:g.139569164C>A , CM000671.1:g.139569164C>A	GRCh37
NC_000009.10:g.138688985C>A	NCBI36
NG_008090.1:g.17748G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.661+23G>T MANE Select	ENSP00000360761.2:n.661+23G>T
ENST00000371694.7:c.565+23G>T	ENSP00000360759.3:n.565+23G>T
ENST00000371696.6:c.661+23G>T	ENSP00000360761.2:n.661+23G>T
ENST00000472820.1:n.589+23G>T
ENST00000538402.1:c.661+23G>T	ENSP00000438919.1:n.661+23G>T
NM_001012727.1:c.565+23G>T	NP_001012745.1:n.565+23G>T
NM_006412.3:c.661+23G>T	NP_006403.2:n.661+23G>T
NM_006412.4:c.661+23G>T MANE Select	NP_006403.2:n.661+23G>T
NM_001012727.2:c.565+23G>T	NP_001012745.1:n.565+23G>T