Canonical Allele Identifier: CA2668886442
Gene: EHHADH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254246_185254247insAGATCGGAAGAGCT , CM000665.2:g.185254246_185254247insAGATCGGAAGAGCT GRCh38
NC_000003.11:g.184972034_184972035insAGATCGGAAGAGCT , CM000665.1:g.184972034_184972035insAGATCGGAAGAGCT GRCh37
NC_000003.10:g.186454728_186454729insAGATCGGAAGAGCT NCBI36
NG_015999.1:g.4852_4853insAGCTCTTCCGATCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5730_228-5729insAGCTCTTCCGATCT
XM_011512517.1:c.-214-5730_-214-5729insAGCTCTTCCGATCT XP_011510819.1:n.-214-5730_-214-5729insAGCTCTTCCGATCT