Canonical Allele Identifier: CA1619457427
Gene: AGPAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177494A= , CM000668.2:g.32177494A= GRCh38
NC_000006.11:g.32145271A= , CM000668.1:g.32145271A= GRCh37
NC_000006.10:g.32253249A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+507T= ENSP00000337463.6:n.-10+507T=
ENST00000395497.5:c.-10+50T= ENSP00000378875.1:n.-10+50T=
NM_032741.4:c.-10+507T= NP_116130.2:n.-10+507T=
XM_011514234.1:c.-10+50T= XP_011512536.1:n.-10+50T=
XM_005248806.2:c.-270T= XP_005248863.1:n.-270T=
NM_032741.5:c.-10+507T= NP_116130.2:n.-10+507T=