Canonical Allele Identifier: CA1619457485
Gene: AGPAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177626C= , CM000668.2:g.32177626C= GRCh38
NC_000006.11:g.32145403C= , CM000668.1:g.32145403C= GRCh37
NC_000006.10:g.32253381C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000336984.6:c.-10+375G= ENSP00000337463.6:n.-10+375G=
ENST00000395497.5:c.-92G= ENSP00000378875.1:n.-92G=
NM_032741.4:c.-10+375G= NP_116130.2:n.-10+375G=
XM_011514234.1:c.-92G= XP_011512536.1:n.-92G=
XM_005248806.2:c.-402G= XP_005248863.1:n.-402G=
NM_032741.5:c.-10+375G= NP_116130.2:n.-10+375G=