Canonical Allele Identifier: CA1619457452
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1785686518

Genomic Alleles

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

Transcript Alleles

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