Canonical Allele Identifier: CA1882796845
Gene: SARDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133671604C= , CM000671.2:g.133671604C= GRCh38
NC_000009.11:g.136536726C= , CM000671.1:g.136536726C= GRCh37
NC_000009.10:g.135526547C= NCBI36
NG_008987.1:g.73352G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000439388.6:c.2257G= MANE Select ENSP00000403084.1:p.Ala753=
ENST00000371868.5:c.541G= ENSP00000360934.1:p.Ala181=
ENST00000371872.8:c.2257G= ENSP00000360938.4:p.Ala753=
ENST00000422262.6:c.1417G= ENSP00000415537.3:p.Ala473=
ENST00000439388.5:c.2257G= ENSP00000403084.1:p.Ala753=
NM_001134707.1:c.2257G= NP_001128179.1:p.Ala753=
NM_007101.3:c.2257G= NP_009032.2:p.Ala753=
XM_006716990.2:c.2257G= XP_006717053.1:p.Ala753=
XM_011518333.1:c.2257G= XP_011516635.1:p.Ala753=
XR_929726.1:n.2424G=
XR_929727.1:n.2424G=
XR_929728.1:n.2424G=
XM_017014367.1:c.2257G= XP_016869856.1:p.Ala753=
XM_017014368.1:c.2257G= XP_016869857.1:p.Ala753=
XR_001746213.1:n.2553G=
XR_001746214.1:n.3736G=
XR_001746215.1:n.2555G=
XR_001746216.1:n.2553G=
XR_001746217.1:n.2553G=
XR_001746218.1:n.2405G=
XR_002956762.1:n.2509G=
XR_929726.2:n.2424G=
NM_001134707.2:c.2257G= MANE Select NP_001128179.1:p.Ala753=
NM_007101.4:c.2257G= NP_009032.2:p.Ala753=