Canonical Allele Identifier: CA375426704
Gene: SARDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133730129C>A , CM000671.2:g.133730129C>A GRCh38
NC_000009.11:g.136595251C>A , CM000671.1:g.136595251C>A GRCh37
NC_000009.10:g.135585072C>A NCBI36
NG_008987.1:g.14827G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000439388.6:c.749G>T MANE Select ENSP00000403084.1:p.Arg250Leu
ENST00000298628.6:c.749G>T ENSP00000298628.5:p.Arg250Leu
ENST00000371867.5:c.482G>T ENSP00000360933.1:p.Arg161Leu
ENST00000371872.8:c.749G>T ENSP00000360938.4:p.Arg250Leu
ENST00000422262.6:c.-92G>T ENSP00000415537.3:n.-92G>T
ENST00000427237.6:c.749G>T ENSP00000394210.2:p.Arg250Leu
ENST00000439388.5:c.749G>T ENSP00000403084.1:p.Arg250Leu
ENST00000616662.4:c.749G>T ENSP00000484683.1:p.Arg250Leu
NM_001134707.1:c.749G>T NP_001128179.1:p.Arg250Leu
NM_007101.3:c.749G>T NP_009032.2:p.Arg250Leu
XM_006716990.2:c.749G>T XP_006717053.1:p.Arg250Leu
XM_011518333.1:c.749G>T XP_011516635.1:p.Arg250Leu
XR_929726.1:n.916G>T
XR_929727.1:n.916G>T
XR_929728.1:n.916G>T
XM_017014367.1:c.749G>T XP_016869856.1:p.Arg250Leu
XM_017014368.1:c.749G>T XP_016869857.1:p.Arg250Leu
XR_001746213.1:n.1045G>T
XR_001746214.1:n.2228G>T
XR_001746215.1:n.1047G>T
XR_001746216.1:n.1045G>T
XR_001746217.1:n.1045G>T
XR_001746218.1:n.1045G>T
XR_929726.2:n.916G>T
NM_001134707.2:c.749G>T MANE Select NP_001128179.1:p.Arg250Leu
NM_007101.4:c.749G>T NP_009032.2:p.Arg250Leu