Canonical Allele Identifier: CA375580658

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139571035A>G (hg19) ; chr9:g.136676583A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676583A>G , CM000671.2:g.136676583A>G	GRCh38
NC_000009.11:g.139571035A>G , CM000671.1:g.139571035A>G	GRCh37
NC_000009.10:g.138690856A>G	NCBI36
NG_008090.1:g.15877T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.588+2T>C MANE Select	ENSP00000360761.2:n.588+2T>C
ENST00000371694.7:c.492+378T>C	ENSP00000360759.3:n.492+378T>C
ENST00000371696.6:c.588+2T>C	ENSP00000360761.2:n.588+2T>C
ENST00000472820.1:n.516+2T>C
ENST00000538402.1:c.588+2T>C	ENSP00000438919.1:n.588+2T>C
NM_001012727.1:c.492+378T>C	NP_001012745.1:n.492+378T>C
NM_006412.3:c.588+2T>C	NP_006403.2:n.588+2T>C
NM_006412.4:c.588+2T>C MANE Select	NP_006403.2:n.588+2T>C
NM_001012727.2:c.492+378T>C	NP_001012745.1:n.492+378T>C