Canonical Allele Identifier: CA1619457443
Gene: AGPAT1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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