Canonical Allele Identifier: CA2497275507
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846047830

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673858_136673861dup , CM000671.2:g.136673858_136673861dup GRCh38
NC_000009.11:g.139568310_139568313dup , CM000671.1:g.139568310_139568313dup GRCh37
NC_000009.10:g.138688131_138688134dup NCBI36
NG_008090.1:g.18601_18604dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.730_733dup MANE Select ENSP00000360761.2:p.Val245AlafsTer?
ENST00000371694.7:c.634_637dup ENSP00000360759.3:p.Val213AlafsTer?
ENST00000371696.6:c.730_733dup ENSP00000360761.2:p.Val245AlafsTer?
ENST00000472820.1:n.658_661dup
ENST00000538402.1:c.730_733dup ENSP00000438919.1:p.Val245AlafsTer?
NM_001012727.1:c.634_637dup NP_001012745.1:p.Val213AlafsTer?
NM_006412.3:c.730_733dup NP_006403.2:p.Val245AlafsTer?
NM_006412.4:c.730_733dup MANE Select NP_006403.2:p.Val245AlafsTer?
NM_001012727.2:c.634_637dup NP_001012745.1:p.Val213AlafsTer?