Canonical Allele Identifier: CA2067555435

Gene: ACADS

Linked Data

• dbSNP Id: rs1861646863

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120738678_120738680del , CM000674.2:g.120738678_120738680del	GRCh38
NC_000012.11:g.121176481_121176483del , CM000674.1:g.121176481_121176483del	GRCh37
NC_000012.10:g.119660864_119660866del	NCBI36
NG_007991.1:g.17911_17913del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242592.9:c.933+8_933+10del MANE Select	ENSP00000242592.4:n.933+8_933+10del
ENST00000242592.8:c.933+8_933+10del	ENSP00000242592.4:n.933+8_933+10del
ENST00000411593.2:c.921+8_921+10del	ENSP00000401045.2:n.921+8_921+10del
NM_000017.3:c.933+8_933+10del	NP_000008.1:n.933+8_933+10del
NM_001302554.1:c.921+8_921+10del	NP_001289483.1:n.921+8_921+10del
NM_000017.4:c.933+8_933+10del MANE Select	NP_000008.1:n.933+8_933+10del
NM_001302554.2:c.921+8_921+10del	NP_001289483.1:n.921+8_921+10del