Canonical Allele Identifier: CA5314642
Gene: SARDH HGNC NCBI

Linked Data

dbSNP Id: rs775898876

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133729846del , CM000671.2:g.133729846del GRCh38
NC_000009.11:g.136594968del , CM000671.1:g.136594968del GRCh37
NC_000009.10:g.135584789del NCBI36
NG_008987.1:g.15112del

Transcript Alleles

HGVS Amino-acid Change
ENST00000439388.6:c.836del MANE Select ENSP00000403084.1:p.Gly279AlafsTer?
ENST00000298628.6:c.836del ENSP00000298628.5:p.Gly279AlafsTer?
ENST00000371867.5:c.569del ENSP00000360933.1:p.Gly190AlafsTer?
ENST00000371872.8:c.836del ENSP00000360938.4:p.Gly279AlafsTer?
ENST00000422262.6:c.-5del ENSP00000415537.3:n.-5del
ENST00000427237.6:c.836del ENSP00000394210.2:p.Gly279AlafsTer?
ENST00000439388.5:c.836del ENSP00000403084.1:p.Gly279AlafsTer?
ENST00000616662.4:c.836del ENSP00000484683.1:p.Gly279AlafsTer?
NM_001134707.1:c.836del NP_001128179.1:p.Gly279AlafsTer?
NM_007101.3:c.836del NP_009032.2:p.Gly279AlafsTer?
XM_006716990.2:c.836del XP_006717053.1:p.Gly279AlafsTer?
XM_011518333.1:c.836del XP_011516635.1:p.Gly279AlafsTer?
XR_929726.1:n.1003del
XR_929727.1:n.1003del
XR_929728.1:n.1003del
XM_017014367.1:c.836del XP_016869856.1:p.Gly279AlafsTer?
XM_017014368.1:c.836del XP_016869857.1:p.Gly279AlafsTer?
XR_001746213.1:n.1132del
XR_001746214.1:n.2315del
XR_001746215.1:n.1134del
XR_001746216.1:n.1132del
XR_001746217.1:n.1132del
XR_001746218.1:n.1132del
XR_929726.2:n.1003del
NM_001134707.2:c.836del MANE Select NP_001128179.1:p.Gly279AlafsTer?
NM_007101.4:c.836del NP_009032.2:p.Gly279AlafsTer?