Canonical Allele Identifier: CA375577216
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673816T>A , CM000671.2:g.136673816T>A GRCh38
NC_000009.11:g.139568268T>A , CM000671.1:g.139568268T>A GRCh37
NC_000009.10:g.138688089T>A NCBI36
NG_008090.1:g.18644A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.773A>T MANE Select ENSP00000360761.2:p.His258Leu
ENST00000371694.7:c.677A>T ENSP00000360759.3:p.His226Leu
ENST00000371696.6:c.773A>T ENSP00000360761.2:p.His258Leu
ENST00000472820.1:n.701A>T
ENST00000538402.1:c.773A>T ENSP00000438919.1:p.His258Leu
NM_001012727.1:c.677A>T NP_001012745.1:p.His226Leu
NM_006412.3:c.773A>T NP_006403.2:p.His258Leu
NM_006412.4:c.773A>T MANE Select NP_006403.2:p.His258Leu
NM_001012727.2:c.677A>T NP_001012745.1:p.His226Leu