Canonical Allele Identifier: CA375578646

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674780-A-G
• MyVariant Identifiers: chr9:g.139569232A>G (hg19) ; chr9:g.136674780A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674780A>G , CM000671.2:g.136674780A>G	GRCh38
NC_000009.11:g.139569232A>G , CM000671.1:g.139569232A>G	GRCh37
NC_000009.10:g.138689053A>G	NCBI36
NG_008090.1:g.17680T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.616T>C MANE Select	ENSP00000360761.2:p.Ser206Pro
ENST00000371694.7:c.520T>C	ENSP00000360759.3:p.Ser174Pro
ENST00000371696.6:c.616T>C	ENSP00000360761.2:p.Ser206Pro
ENST00000472820.1:n.544T>C
ENST00000538402.1:c.616T>C	ENSP00000438919.1:p.Ser206Pro
NM_001012727.1:c.520T>C	NP_001012745.1:p.Ser174Pro
NM_006412.3:c.616T>C	NP_006403.2:p.Ser206Pro
NM_006412.4:c.616T>C MANE Select	NP_006403.2:p.Ser206Pro
NM_001012727.2:c.520T>C	NP_001012745.1:p.Ser174Pro