Canonical Allele Identifier: CA136908701
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs17493811
gnomAD v2: 6-32145399-C-G
gnomAD v3: 6-32177622-C-G
gnomAD v4: 6-32177622-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177622C>G , CM000668.2:g.32177622C>G GRCh38
NC_000006.11:g.32145399C>G , CM000668.1:g.32145399C>G GRCh37
NC_000006.10:g.32253377C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000336984.6:c.-10+379G>C ENSP00000337463.6:n.-10+379G>C
ENST00000395497.5:c.-88G>C ENSP00000378875.1:n.-88G>C
NM_032741.4:c.-10+379G>C NP_116130.2:n.-10+379G>C
XM_011514234.1:c.-88G>C XP_011512536.1:n.-88G>C
XM_005248806.2:c.-398G>C XP_005248863.1:n.-398G>C
NM_032741.5:c.-10+379G>C NP_116130.2:n.-10+379G>C