Canonical Allele Identifier: CA566372825
Gene: AGPAT1 HGNC NCBI

Linked Data

gnomAD v2: 6-32145433-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177656A>C , CM000668.2:g.32177656A>C GRCh38
NC_000006.11:g.32145433A>C , CM000668.1:g.32145433A>C GRCh37
NC_000006.10:g.32253411A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000336984.6:c.-10+345T>G ENSP00000337463.6:n.-10+345T>G
ENST00000395497.5:c.-122T>G ENSP00000378875.1:n.-122T>G
NM_032741.4:c.-10+345T>G NP_116130.2:n.-10+345T>G
XM_011514234.1:c.-122T>G XP_011512536.1:n.-122T>G
XM_005248806.2:c.-432T>G XP_005248863.1:n.-432T>G
NM_032741.5:c.-10+345T>G NP_116130.2:n.-10+345T>G