Canonical Allele Identifier: CA1087505901
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1785684126
gnomAD v3: 6-32177526-T-C
gnomAD v4: 6-32177526-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177526T>C , CM000668.2:g.32177526T>C GRCh38
NC_000006.11:g.32145303T>C , CM000668.1:g.32145303T>C GRCh37
NC_000006.10:g.32253281T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000336984.6:c.-10+475A>G ENSP00000337463.6:n.-10+475A>G
ENST00000395497.5:c.-10+18A>G ENSP00000378875.1:n.-10+18A>G
NM_032741.4:c.-10+475A>G NP_116130.2:n.-10+475A>G
XM_011514234.1:c.-10+18A>G XP_011512536.1:n.-10+18A>G
XM_005248806.2:c.-302A>G XP_005248863.1:n.-302A>G
NM_032741.5:c.-10+475A>G NP_116130.2:n.-10+475A>G