Canonical Allele Identifier: CA1619457453
Gene: AGPAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177550T= , CM000668.2:g.32177550T= GRCh38
NC_000006.11:g.32145327T= , CM000668.1:g.32145327T= GRCh37
NC_000006.10:g.32253305T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000336984.6:c.-10+451A= ENSP00000337463.6:n.-10+451A=
ENST00000395497.5:c.-16A= ENSP00000378875.1:n.-16A=
NM_032741.4:c.-10+451A= NP_116130.2:n.-10+451A=
XM_011514234.1:c.-16A= XP_011512536.1:n.-16A=
XM_005248806.2:c.-326A= XP_005248863.1:n.-326A=
NM_032741.5:c.-10+451A= NP_116130.2:n.-10+451A=