Canonical Allele Identifier: CA375577613
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136673894-G-A
MyVariant Identifiers: chr9:g.139568346G>A (hg19) chr9:g.136673894G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673894G>A , CM000671.2:g.136673894G>A GRCh38
NC_000009.11:g.139568346G>A , CM000671.1:g.139568346G>A GRCh37
NC_000009.10:g.138688167G>A NCBI36
NG_008090.1:g.18566C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.695C>T MANE Select ENSP00000360761.2:p.Pro232Leu
ENST00000371694.7:c.599C>T ENSP00000360759.3:p.Pro200Leu
ENST00000371696.6:c.695C>T ENSP00000360761.2:p.Pro232Leu
ENST00000472820.1:n.623C>T
ENST00000538402.1:c.695C>T ENSP00000438919.1:p.Pro232Leu
NM_001012727.1:c.599C>T NP_001012745.1:p.Pro200Leu
NM_006412.3:c.695C>T NP_006403.2:p.Pro232Leu
NM_006412.4:c.695C>T MANE Select NP_006403.2:p.Pro232Leu
NM_001012727.2:c.599C>T NP_001012745.1:p.Pro200Leu
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