Canonical Allele Identifier: CA386613949
Gene: ACADS HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.121174801G>A (hg19) chr12:g.120736998G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120736998G>A , CM000674.2:g.120736998G>A GRCh38
NC_000012.11:g.121174801G>A , CM000674.1:g.121174801G>A GRCh37
NC_000012.10:g.119659184G>A NCBI36
NG_007991.1:g.16231G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.223G>A MANE Select ENSP00000242592.4:p.Gly75Ser
ENST00000242592.8:c.223G>A ENSP00000242592.4:p.Gly75Ser
ENST00000411593.2:c.223G>A ENSP00000401045.2:p.Gly75Ser
ENST00000539690.1:n.335G>A
NM_000017.3:c.223G>A NP_000008.1:p.Gly75Ser
NM_001302554.1:c.223G>A NP_001289483.1:p.Gly75Ser
NM_000017.4:c.223G>A MANE Select NP_000008.1:p.Gly75Ser
NM_001302554.2:c.223G>A NP_001289483.1:p.Gly75Ser
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