Canonical Allele Identifier: CA2692653738

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136673746-TCTGGGCTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673753_136673760del , CM000671.2:g.136673753_136673760del	GRCh38
NC_000009.11:g.139568205_139568212del , CM000671.1:g.139568205_139568212del	GRCh37
NC_000009.10:g.138688026_138688033del	NCBI36
NG_008090.1:g.18706_18713del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.835_*5del MANE Select	ENSP00000360761.2:n.[c.835_*5del;Ter279ThrextTer?]
ENST00000371694.7:c.739_*5del	ENSP00000360759.3:n.[c.739_*5del;Ter247ThrextTer?]
ENST00000371696.6:c.835_*5del	ENSP00000360761.2:n.[c.835_*5del;Ter279ThrextTer?]
ENST00000472820.1:n.763_770del
ENST00000538402.1:c.835_*5del	ENSP00000438919.1:n.[c.835_*5del;Ter279ThrextTer?]
NM_001012727.1:c.739_*5del	NP_001012745.1:n.[c.739_*5del;Ter247ThrextTer?]
NM_006412.3:c.835_*5del	NP_006403.2:n.[c.835_*5del;Ter279ThrextTer?]
NM_006412.4:c.835_*5del MANE Select	NP_006403.2:n.[c.835_*5del;Ter279ThrextTer?]
NM_001012727.2:c.739_*5del	NP_001012745.1:n.[c.739_*5del;Ter247ThrextTer?]