Canonical Allele Identifier: CA375426809
Gene: SARDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133730178T>G , CM000671.2:g.133730178T>G GRCh38
NC_000009.11:g.136595300T>G , CM000671.1:g.136595300T>G GRCh37
NC_000009.10:g.135585121T>G NCBI36
NG_008987.1:g.14778A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000439388.6:c.700A>C MANE Select ENSP00000403084.1:p.Asn234His
ENST00000298628.6:c.700A>C ENSP00000298628.5:p.Asn234His
ENST00000371867.5:c.433A>C ENSP00000360933.1:p.Asn145His
ENST00000371872.8:c.700A>C ENSP00000360938.4:p.Asn234His
ENST00000427237.6:c.700A>C ENSP00000394210.2:p.Asn234His
ENST00000439388.5:c.700A>C ENSP00000403084.1:p.Asn234His
ENST00000616662.4:c.700A>C ENSP00000484683.1:p.Asn234His
NM_001134707.1:c.700A>C NP_001128179.1:p.Asn234His
NM_007101.3:c.700A>C NP_009032.2:p.Asn234His
XM_006716990.2:c.700A>C XP_006717053.1:p.Asn234His
XM_011518333.1:c.700A>C XP_011516635.1:p.Asn234His
XR_929726.1:n.867A>C
XR_929727.1:n.867A>C
XR_929728.1:n.867A>C
XM_017014367.1:c.700A>C XP_016869856.1:p.Asn234His
XM_017014368.1:c.700A>C XP_016869857.1:p.Asn234His
XR_001746213.1:n.996A>C
XR_001746214.1:n.2179A>C
XR_001746215.1:n.998A>C
XR_001746216.1:n.996A>C
XR_001746217.1:n.996A>C
XR_001746218.1:n.996A>C
XR_929726.2:n.867A>C
NM_001134707.2:c.700A>C MANE Select NP_001128179.1:p.Asn234His
NM_007101.4:c.700A>C NP_009032.2:p.Asn234His