Canonical Allele Identifier: CA1882796841

Gene: SARDH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133671600G= , CM000671.2:g.133671600G=	GRCh38
NC_000009.11:g.136536722G= , CM000671.1:g.136536722G=	GRCh37
NC_000009.10:g.135526543G=	NCBI36
NG_008987.1:g.73356C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439388.6:c.2261C= MANE Select	ENSP00000403084.1:p.Ala754=
ENST00000371868.5:c.545C=	ENSP00000360934.1:p.Ala182=
ENST00000371872.8:c.2261C=	ENSP00000360938.4:p.Ala754=
ENST00000422262.6:c.1421C=	ENSP00000415537.3:p.Ala474=
ENST00000439388.5:c.2261C=	ENSP00000403084.1:p.Ala754=
NM_001134707.1:c.2261C=	NP_001128179.1:p.Ala754=
NM_007101.3:c.2261C=	NP_009032.2:p.Ala754=
XM_006716990.2:c.2261C=	XP_006717053.1:p.Ala754=
XM_011518333.1:c.2261C=	XP_011516635.1:p.Ala754=
XR_929726.1:n.2428C=
XR_929727.1:n.2428C=
XR_929728.1:n.2428C=
XM_017014367.1:c.2261C=	XP_016869856.1:p.Ala754=
XM_017014368.1:c.2261C=	XP_016869857.1:p.Ala754=
XR_001746213.1:n.2557C=
XR_001746214.1:n.3740C=
XR_001746215.1:n.2559C=
XR_001746216.1:n.2557C=
XR_001746217.1:n.2557C=
XR_001746218.1:n.2409C=
XR_002956762.1:n.2513C=
XR_929726.2:n.2428C=
NM_001134707.2:c.2261C= MANE Select	NP_001128179.1:p.Ala754=
NM_007101.4:c.2261C=	NP_009032.2:p.Ala754=