Canonical Allele Identifier: CA375426681
Gene: SARDH HGNC NCBI

Linked Data

dbSNP Id: rs749045238

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133730115C>A , CM000671.2:g.133730115C>A GRCh38
NC_000009.11:g.136595237C>A , CM000671.1:g.136595237C>A GRCh37
NC_000009.10:g.135585058C>A NCBI36
NG_008987.1:g.14841G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000439388.6:c.763G>T MANE Select ENSP00000403084.1:p.Val255Leu
ENST00000298628.6:c.763G>T ENSP00000298628.5:p.Val255Leu
ENST00000371867.5:c.496G>T ENSP00000360933.1:p.Val166Leu
ENST00000371872.8:c.763G>T ENSP00000360938.4:p.Val255Leu
ENST00000422262.6:c.-78G>T ENSP00000415537.3:n.-78G>T
ENST00000427237.6:c.763G>T ENSP00000394210.2:p.Val255Leu
ENST00000439388.5:c.763G>T ENSP00000403084.1:p.Val255Leu
ENST00000616662.4:c.763G>T ENSP00000484683.1:p.Val255Leu
NM_001134707.1:c.763G>T NP_001128179.1:p.Val255Leu
NM_007101.3:c.763G>T NP_009032.2:p.Val255Leu
XM_006716990.2:c.763G>T XP_006717053.1:p.Val255Leu
XM_011518333.1:c.763G>T XP_011516635.1:p.Val255Leu
XR_929726.1:n.930G>T
XR_929727.1:n.930G>T
XR_929728.1:n.930G>T
XM_017014367.1:c.763G>T XP_016869856.1:p.Val255Leu
XM_017014368.1:c.763G>T XP_016869857.1:p.Val255Leu
XR_001746213.1:n.1059G>T
XR_001746214.1:n.2242G>T
XR_001746215.1:n.1061G>T
XR_001746216.1:n.1059G>T
XR_001746217.1:n.1059G>T
XR_001746218.1:n.1059G>T
XR_929726.2:n.930G>T
NM_001134707.2:c.763G>T MANE Select NP_001128179.1:p.Val255Leu
NM_007101.4:c.763G>T NP_009032.2:p.Val255Leu