Canonical Allele Identifier: CA2692402503
Gene: SARDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133730080_133730099del , CM000671.2:g.133730080_133730099del GRCh38
NC_000009.11:g.136595202_136595221del , CM000671.1:g.136595202_136595221del GRCh37
NC_000009.10:g.135585023_135585042del NCBI36
NG_008987.1:g.14859_14878del

Transcript Alleles

HGVS Amino-acid Change
ENST00000439388.6:c.781_800del MANE Select ENSP00000403084.1:p.Ser261GlyfsTer?
ENST00000298628.6:c.781_800del ENSP00000298628.5:p.Ser261GlyfsTer?
ENST00000371867.5:c.514_533del ENSP00000360933.1:p.Ser172GlyfsTer?
ENST00000371872.8:c.781_800del ENSP00000360938.4:p.Ser261GlyfsTer?
ENST00000422262.6:c.-60_-41del ENSP00000415537.3:n.-60_-41del
ENST00000427237.6:c.781_800del ENSP00000394210.2:p.Ser261GlyfsTer?
ENST00000439388.5:c.781_800del ENSP00000403084.1:p.Ser261GlyfsTer?
ENST00000616662.4:c.781_800del ENSP00000484683.1:p.Ser261GlyfsTer?
NM_001134707.1:c.781_800del NP_001128179.1:p.Ser261GlyfsTer?
NM_007101.3:c.781_800del NP_009032.2:p.Ser261GlyfsTer?
XM_006716990.2:c.781_800del XP_006717053.1:p.Ser261GlyfsTer?
XM_011518333.1:c.781_800del XP_011516635.1:p.Ser261GlyfsTer?
XR_929726.1:n.948_967del
XR_929727.1:n.948_967del
XR_929728.1:n.948_967del
XM_017014367.1:c.781_800del XP_016869856.1:p.Ser261GlyfsTer?
XM_017014368.1:c.781_800del XP_016869857.1:p.Ser261GlyfsTer?
XR_001746213.1:n.1077_1096del
XR_001746214.1:n.2260_2279del
XR_001746215.1:n.1079_1098del
XR_001746216.1:n.1077_1096del
XR_001746217.1:n.1077_1096del
XR_001746218.1:n.1077_1096del
XR_929726.2:n.948_967del
NM_001134707.2:c.781_800del MANE Select NP_001128179.1:p.Ser261GlyfsTer?
NM_007101.4:c.781_800del NP_009032.2:p.Ser261GlyfsTer?