Canonical Allele Identifier: CA1619457491
Gene: AGPAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177635A= , CM000668.2:g.32177635A= GRCh38
NC_000006.11:g.32145412A= , CM000668.1:g.32145412A= GRCh37
NC_000006.10:g.32253390A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+366T= ENSP00000337463.6:n.-10+366T=
ENST00000395497.5:c.-101T= ENSP00000378875.1:n.-101T=
NM_032741.4:c.-10+366T= NP_116130.2:n.-10+366T=
XM_011514234.1:c.-101T= XP_011512536.1:n.-101T=
XM_005248806.2:c.-411T= XP_005248863.1:n.-411T=
NM_032741.5:c.-10+366T= NP_116130.2:n.-10+366T=