Canonical Allele Identifier: CA1619457439
Gene: AGPAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177515C= , CM000668.2:g.32177515C= GRCh38
NC_000006.11:g.32145292C= , CM000668.1:g.32145292C= GRCh37
NC_000006.10:g.32253270C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+486G= ENSP00000337463.6:n.-10+486G=
ENST00000395497.5:c.-10+29G= ENSP00000378875.1:n.-10+29G=
NM_032741.4:c.-10+486G= NP_116130.2:n.-10+486G=
XM_011514234.1:c.-10+29G= XP_011512536.1:n.-10+29G=
XM_005248806.2:c.-291G= XP_005248863.1:n.-291G=
NM_032741.5:c.-10+486G= NP_116130.2:n.-10+486G=