Canonical Allele Identifier: CA1619457399
Gene: AGPAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177438T= , CM000668.2:g.32177438T= GRCh38
NC_000006.11:g.32145215T= , CM000668.1:g.32145215T= GRCh37
NC_000006.10:g.32253193T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+563A= ENSP00000337463.6:n.-10+563A=
ENST00000395497.5:c.-10+106A= ENSP00000378875.1:n.-10+106A=
NM_032741.4:c.-10+563A= NP_116130.2:n.-10+563A=
XM_011514234.1:c.-10+106A= XP_011512536.1:n.-10+106A=
XM_005248806.2:c.-214A= XP_005248863.1:n.-214A=
NM_032741.5:c.-10+563A= NP_116130.2:n.-10+563A=