Canonical Allele Identifier: CA2770519926
Gene: AGPAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177816C>T , CM000668.2:g.32177816C>T GRCh38
NC_000006.11:g.32145593C>T , CM000668.1:g.32145593C>T GRCh37
NC_000006.10:g.32253571C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+185G>A ENSP00000337463.6:n.-10+185G>A
NM_032741.4:c.-10+185G>A NP_116130.2:n.-10+185G>A
XM_011514234.1:c.-282G>A XP_011512536.1:n.-282G>A
NM_032741.5:c.-10+185G>A NP_116130.2:n.-10+185G>A