Canonical Allele Identifier: CA375576131

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136673774-G-T
• MyVariant Identifiers: chr9:g.139568226G>T (hg19) ; chr9:g.136673774G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673774G>T , CM000671.2:g.136673774G>T	GRCh38
NC_000009.11:g.139568226G>T , CM000671.1:g.139568226G>T	GRCh37
NC_000009.10:g.138688047G>T	NCBI36
NG_008090.1:g.18686C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.815C>A MANE Select	ENSP00000360761.2:p.Ser272Tyr
ENST00000371694.7:c.719C>A	ENSP00000360759.3:p.Ser240Tyr
ENST00000371696.6:c.815C>A	ENSP00000360761.2:p.Ser272Tyr
ENST00000472820.1:n.743C>A
ENST00000538402.1:c.815C>A	ENSP00000438919.1:p.Ser272Tyr
NM_001012727.1:c.719C>A	NP_001012745.1:p.Ser240Tyr
NM_006412.3:c.815C>A	NP_006403.2:p.Ser272Tyr
NM_006412.4:c.815C>A MANE Select	NP_006403.2:p.Ser272Tyr
NM_001012727.2:c.719C>A	NP_001012745.1:p.Ser240Tyr