Canonical Allele Identifier: CA2579502515
Gene: SARDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133729741del , CM000671.2:g.133729741del GRCh38
NC_000009.11:g.136594863del , CM000671.1:g.136594863del GRCh37
NC_000009.10:g.135584684del NCBI36
NG_008987.1:g.15215del

Transcript Alleles

HGVS Amino-acid change
ENST00000439388.6:c.915+24del MANE Select ENSP00000403084.1:n.915+24del
ENST00000298628.6:c.915+24del ENSP00000298628.5:n.915+24del
ENST00000371867.5:c.648+24del ENSP00000360933.1:n.648+24del
ENST00000371872.8:c.915+24del ENSP00000360938.4:n.915+24del
ENST00000422262.6:c.75+24del ENSP00000415537.3:n.75+24del
ENST00000427237.6:c.915+24del ENSP00000394210.2:n.915+24del
ENST00000439388.5:c.915+24del ENSP00000403084.1:n.915+24del
ENST00000616662.4:c.915+24del ENSP00000484683.1:n.915+24del
NM_001134707.1:c.915+24del NP_001128179.1:n.915+24del
NM_007101.3:c.915+24del NP_009032.2:n.915+24del
XM_006716990.2:c.915+24del XP_006717053.1:n.915+24del
XM_011518333.1:c.915+24del XP_011516635.1:n.915+24del
XR_929726.1:n.1082+24del
XR_929727.1:n.1082+24del
XR_929728.1:n.1082+24del
XM_017014367.1:c.915+24del XP_016869856.1:n.915+24del
XM_017014368.1:c.915+24del XP_016869857.1:n.915+24del
XR_001746213.1:n.1211+24del
XR_001746214.1:n.2394+24del
XR_001746215.1:n.1213+24del
XR_001746216.1:n.1211+24del
XR_001746217.1:n.1211+24del
XR_001746218.1:n.1211+24del
XR_929726.2:n.1082+24del
NM_001134707.2:c.915+24del MANE Select NP_001128179.1:n.915+24del
NM_007101.4:c.915+24del NP_009032.2:n.915+24del