Canonical Allele Identifier: CA201627646
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs944239002

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674754C>T , CM000671.2:g.136674754C>T GRCh38
NC_000009.11:g.139569206C>T , CM000671.1:g.139569206C>T GRCh37
NC_000009.10:g.138689027C>T NCBI36
NG_008090.1:g.17706G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.642G>A MANE Select ENSP00000360761.2:p.Lys214=
ENST00000371694.7:c.546G>A ENSP00000360759.3:p.Lys182=
ENST00000371696.6:c.642G>A ENSP00000360761.2:p.Lys214=
ENST00000472820.1:n.570G>A
ENST00000538402.1:c.642G>A ENSP00000438919.1:p.Lys214=
NM_001012727.1:c.546G>A NP_001012745.1:p.Lys182=
NM_006412.3:c.642G>A NP_006403.2:p.Lys214=
NM_006412.4:c.642G>A MANE Select NP_006403.2:p.Lys214=
NM_001012727.2:c.546G>A NP_001012745.1:p.Lys182=