Canonical Allele Identifier: CA1619457579
Gene: AGPAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177819A= , CM000668.2:g.32177819A= GRCh38
NC_000006.11:g.32145596A= , CM000668.1:g.32145596A= GRCh37
NC_000006.10:g.32253574A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+182T= ENSP00000337463.6:n.-10+182T=
NM_032741.4:c.-10+182T= NP_116130.2:n.-10+182T=
XM_011514234.1:c.-285T= XP_011512536.1:n.-285T=
NM_032741.5:c.-10+182T= NP_116130.2:n.-10+182T=