Canonical Allele Identifier: CA386601695
Gene: ACADS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739173G>T , CM000674.2:g.120739173G>T GRCh38
NC_000012.11:g.121176976G>T , CM000674.1:g.121176976G>T GRCh37
NC_000012.10:g.119661359G>T NCBI36
NG_007991.1:g.18406G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.1063G>T MANE Select ENSP00000242592.4:p.Ala355Ser
ENST00000242592.8:c.1063G>T ENSP00000242592.4:p.Ala355Ser
ENST00000411593.2:c.1051G>T ENSP00000401045.2:p.Ala351Ser
NM_000017.3:c.1063G>T NP_000008.1:p.Ala355Ser
NM_001302554.1:c.1051G>T NP_001289483.1:p.Ala351Ser
NM_000017.4:c.1063G>T MANE Select NP_000008.1:p.Ala355Ser
NM_001302554.2:c.1051G>T NP_001289483.1:p.Ala351Ser