Canonical Allele Identifier: CA2678121452
Gene: AGPAT1 HGNC NCBI

Linked Data

gnomAD v4: 6-32177522-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177522T>C , CM000668.2:g.32177522T>C GRCh38
NC_000006.11:g.32145299T>C , CM000668.1:g.32145299T>C GRCh37
NC_000006.10:g.32253277T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000336984.6:c.-10+479A>G ENSP00000337463.6:n.-10+479A>G
ENST00000395497.5:c.-10+22A>G ENSP00000378875.1:n.-10+22A>G
NM_032741.4:c.-10+479A>G NP_116130.2:n.-10+479A>G
XM_011514234.1:c.-10+22A>G XP_011512536.1:n.-10+22A>G
XM_005248806.2:c.-298A>G XP_005248863.1:n.-298A>G
NM_032741.5:c.-10+479A>G NP_116130.2:n.-10+479A>G