Canonical Allele Identifier: CA2067556028
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1883598625

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739716C>T , CM000674.2:g.120739716C>T GRCh38
NC_000012.11:g.121177519C>T , CM000674.1:g.121177519C>T GRCh37
NC_000012.10:g.119661902C>T NCBI36
NG_007991.1:g.18949C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*268C>T MANE Select ENSP00000242592.4:n.*268C>T
ENST00000242592.8:c.*268C>T ENSP00000242592.4:n.*268C>T
NM_000017.3:c.*268C>T NP_000008.1:n.*268C>T
NM_001302554.1:c.*268C>T NP_001289483.1:n.*268C>T
NM_000017.4:c.*268C>T MANE Select NP_000008.1:n.*268C>T
NM_001302554.2:c.*268C>T NP_001289483.1:n.*268C>T