Canonical Allele Identifier: CA375578404
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674759T>A , CM000671.2:g.136674759T>A GRCh38
NC_000009.11:g.139569211T>A , CM000671.1:g.139569211T>A GRCh37
NC_000009.10:g.138689032T>A NCBI36
NG_008090.1:g.17701A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.637A>T MANE Select ENSP00000360761.2:p.Thr213Ser
ENST00000371694.7:c.541A>T ENSP00000360759.3:p.Thr181Ser
ENST00000371696.6:c.637A>T ENSP00000360761.2:p.Thr213Ser
ENST00000472820.1:n.565A>T
ENST00000538402.1:c.637A>T ENSP00000438919.1:p.Thr213Ser
NM_001012727.1:c.541A>T NP_001012745.1:p.Thr181Ser
NM_006412.3:c.637A>T NP_006403.2:p.Thr213Ser
NM_006412.4:c.637A>T MANE Select NP_006403.2:p.Thr213Ser
NM_001012727.2:c.541A>T NP_001012745.1:p.Thr181Ser