Canonical Allele Identifier: CA2678121513
Gene: AGPAT1 HGNC NCBI

Linked Data

gnomAD v4: 6-32177645-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177645C>T , CM000668.2:g.32177645C>T GRCh38
NC_000006.11:g.32145422C>T , CM000668.1:g.32145422C>T GRCh37
NC_000006.10:g.32253400C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000336984.6:c.-10+356G>A ENSP00000337463.6:n.-10+356G>A
ENST00000395497.5:c.-111G>A ENSP00000378875.1:n.-111G>A
NM_032741.4:c.-10+356G>A NP_116130.2:n.-10+356G>A
XM_011514234.1:c.-111G>A XP_011512536.1:n.-111G>A
XM_005248806.2:c.-421G>A XP_005248863.1:n.-421G>A
NM_032741.5:c.-10+356G>A NP_116130.2:n.-10+356G>A