Canonical Allele Identifier: CA1087505908
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1785688504
gnomAD v3: 6-32177559-C-T
gnomAD v4: 6-32177559-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177559C>T , CM000668.2:g.32177559C>T GRCh38
NC_000006.11:g.32145336C>T , CM000668.1:g.32145336C>T GRCh37
NC_000006.10:g.32253314C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000336984.6:c.-10+442G>A ENSP00000337463.6:n.-10+442G>A
ENST00000395497.5:c.-25G>A ENSP00000378875.1:n.-25G>A
NM_032741.4:c.-10+442G>A NP_116130.2:n.-10+442G>A
XM_011514234.1:c.-25G>A XP_011512536.1:n.-25G>A
XM_005248806.2:c.-335G>A XP_005248863.1:n.-335G>A
NM_032741.5:c.-10+442G>A NP_116130.2:n.-10+442G>A