Canonical Allele Identifier: CA2692654802

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676913-C-CTGCCTTCTCCCTGGCTACCT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676913_136676914insTGCCTTCTCCCTGGCTACCT , CM000671.2:g.136676913_136676914insTGCCTTCTCCCTGGCTACCT	GRCh38
NC_000009.11:g.139571365_139571366insTGCCTTCTCCCTGGCTACCT , CM000671.1:g.139571365_139571366insTGCCTTCTCCCTGGCTACCT	GRCh37
NC_000009.10:g.138691186_138691187insTGCCTTCTCCCTGGCTACCT	NCBI36
NG_008090.1:g.15546_15547insAGGTAGCCAGGGAGAAGGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+47_492+48insAGGTAGCCAGGGAGAAGGCA MANE Select	ENSP00000360761.2:n.492+47_492+48insAGGTAGCCAGGGAGAAGGCA
ENST00000371694.7:c.492+47_492+48insAGGTAGCCAGGGAGAAGGCA	ENSP00000360759.3:n.492+47_492+48insAGGTAGCCAGGGAGAAGGCA
ENST00000371696.6:c.492+47_492+48insAGGTAGCCAGGGAGAAGGCA	ENSP00000360761.2:n.492+47_492+48insAGGTAGCCAGGGAGAAGGCA
ENST00000472820.1:n.420+47_420+48insAGGTAGCCAGGGAGAAGGCA
ENST00000538402.1:c.492+47_492+48insAGGTAGCCAGGGAGAAGGCA	ENSP00000438919.1:n.492+47_492+48insAGGTAGCCAGGGAGAAGGCA
NM_001012727.1:c.492+47_492+48insAGGTAGCCAGGGAGAAGGCA	NP_001012745.1:n.492+47_492+48insAGGTAGCCAGGGAGAAGGCA
NM_006412.3:c.492+47_492+48insAGGTAGCCAGGGAGAAGGCA	NP_006403.2:n.492+47_492+48insAGGTAGCCAGGGAGAAGGCA
NM_006412.4:c.492+47_492+48insAGGTAGCCAGGGAGAAGGCA MANE Select	NP_006403.2:n.492+47_492+48insAGGTAGCCAGGGAGAAGGCA
NM_001012727.2:c.492+47_492+48insAGGTAGCCAGGGAGAAGGCA	NP_001012745.1:n.492+47_492+48insAGGTAGCCAGGGAGAAGGCA