Canonical Allele Identifier: CA1087505918
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1364096367
gnomAD v3: 6-32177619-A-C
gnomAD v4: 6-32177619-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177619A>C , CM000668.2:g.32177619A>C GRCh38
NC_000006.11:g.32145396A>C , CM000668.1:g.32145396A>C GRCh37
NC_000006.10:g.32253374A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+382T>G ENSP00000337463.6:n.-10+382T>G
ENST00000395497.5:c.-85T>G ENSP00000378875.1:n.-85T>G
NM_032741.4:c.-10+382T>G NP_116130.2:n.-10+382T>G
XM_011514234.1:c.-85T>G XP_011512536.1:n.-85T>G
XM_005248806.2:c.-395T>G XP_005248863.1:n.-395T>G
NM_032741.5:c.-10+382T>G NP_116130.2:n.-10+382T>G