Canonical Allele Identifier: CA5314687
Gene: SARDH HGNC NCBI

Linked Data

dbSNP Id: rs753160140

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133730138A>G , CM000671.2:g.133730138A>G GRCh38
NC_000009.11:g.136595260A>G , CM000671.1:g.136595260A>G GRCh37
NC_000009.10:g.135585081A>G NCBI36
NG_008987.1:g.14818T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000439388.6:c.740T>C MANE Select ENSP00000403084.1:p.Phe247Ser
ENST00000298628.6:c.740T>C ENSP00000298628.5:p.Phe247Ser
ENST00000371867.5:c.473T>C ENSP00000360933.1:p.Phe158Ser
ENST00000371872.8:c.740T>C ENSP00000360938.4:p.Phe247Ser
ENST00000422262.6:c.-101T>C ENSP00000415537.3:n.-101T>C
ENST00000427237.6:c.740T>C ENSP00000394210.2:p.Phe247Ser
ENST00000439388.5:c.740T>C ENSP00000403084.1:p.Phe247Ser
ENST00000616662.4:c.740T>C ENSP00000484683.1:p.Phe247Ser
NM_001134707.1:c.740T>C NP_001128179.1:p.Phe247Ser
NM_007101.3:c.740T>C NP_009032.2:p.Phe247Ser
XM_006716990.2:c.740T>C XP_006717053.1:p.Phe247Ser
XM_011518333.1:c.740T>C XP_011516635.1:p.Phe247Ser
XR_929726.1:n.907T>C
XR_929727.1:n.907T>C
XR_929728.1:n.907T>C
XM_017014367.1:c.740T>C XP_016869856.1:p.Phe247Ser
XM_017014368.1:c.740T>C XP_016869857.1:p.Phe247Ser
XR_001746213.1:n.1036T>C
XR_001746214.1:n.2219T>C
XR_001746215.1:n.1038T>C
XR_001746216.1:n.1036T>C
XR_001746217.1:n.1036T>C
XR_001746218.1:n.1036T>C
XR_929726.2:n.907T>C
NM_001134707.2:c.740T>C MANE Select NP_001128179.1:p.Phe247Ser
NM_007101.4:c.740T>C NP_009032.2:p.Phe247Ser