Canonical Allele Identifier: CA2838660435
Gene: SARDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133729959del , CM000671.2:g.133729959del GRCh38
NC_000009.11:g.136595081del , CM000671.1:g.136595081del GRCh37
NC_000009.10:g.135584902del NCBI36
NG_008987.1:g.14999del

Transcript Alleles

HGVS Amino-acid Change
ENST00000439388.6:c.815-92del MANE Select ENSP00000403084.1:n.815-92del
ENST00000298628.6:c.815-92del ENSP00000298628.5:n.815-92del
ENST00000371867.5:c.548-92del ENSP00000360933.1:n.548-92del
ENST00000371872.8:c.815-92del ENSP00000360938.4:n.815-92del
ENST00000422262.6:c.-26-92del ENSP00000415537.3:n.-26-92del
ENST00000427237.6:c.815-92del ENSP00000394210.2:n.815-92del
ENST00000439388.5:c.815-92del ENSP00000403084.1:n.815-92del
ENST00000616662.4:c.815-92del ENSP00000484683.1:n.815-92del
NM_001134707.1:c.815-92del NP_001128179.1:n.815-92del
NM_007101.3:c.815-92del NP_009032.2:n.815-92del
XM_006716990.2:c.815-92del XP_006717053.1:n.815-92del
XM_011518333.1:c.815-92del XP_011516635.1:n.815-92del
XR_929726.1:n.982-92del
XR_929727.1:n.982-92del
XR_929728.1:n.982-92del
XM_017014367.1:c.815-92del XP_016869856.1:n.815-92del
XM_017014368.1:c.815-92del XP_016869857.1:n.815-92del
XR_001746213.1:n.1111-92del
XR_001746214.1:n.2294-92del
XR_001746215.1:n.1113-92del
XR_001746216.1:n.1111-92del
XR_001746217.1:n.1111-92del
XR_001746218.1:n.1111-92del
XR_929726.2:n.982-92del
NM_001134707.2:c.815-92del MANE Select NP_001128179.1:n.815-92del
NM_007101.4:c.815-92del NP_009032.2:n.815-92del