Canonical Allele Identifier: CA375581306
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676661G>A , CM000671.2:g.136676661G>A GRCh38
NC_000009.11:g.139571113G>A , CM000671.1:g.139571113G>A GRCh37
NC_000009.10:g.138690934G>A NCBI36
NG_008090.1:g.15799C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.512C>T MANE Select ENSP00000360761.2:p.Pro171Leu
ENST00000371694.7:c.492+300C>T ENSP00000360759.3:n.492+300C>T
ENST00000371696.6:c.512C>T ENSP00000360761.2:p.Pro171Leu
ENST00000472820.1:n.440C>T
ENST00000538402.1:c.512C>T ENSP00000438919.1:p.Pro171Leu
NM_001012727.1:c.492+300C>T NP_001012745.1:n.492+300C>T
NM_006412.3:c.512C>T NP_006403.2:p.Pro171Leu
NM_006412.4:c.512C>T MANE Select NP_006403.2:p.Pro171Leu
NM_001012727.2:c.492+300C>T NP_001012745.1:n.492+300C>T