Canonical Allele Identifier: CA1882821247

Gene: SARDH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133730165G= , CM000671.2:g.133730165G=	GRCh38
NC_000009.11:g.136595287G= , CM000671.1:g.136595287G=	GRCh37
NC_000009.10:g.135585108G=	NCBI36
NG_008987.1:g.14791C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439388.6:c.713C= MANE Select	ENSP00000403084.1:p.Thr238=
ENST00000298628.6:c.713C=	ENSP00000298628.5:p.Thr238=
ENST00000371867.5:c.446C=	ENSP00000360933.1:p.Thr149=
ENST00000371872.8:c.713C=	ENSP00000360938.4:p.Thr238=
ENST00000427237.6:c.713C=	ENSP00000394210.2:p.Thr238=
ENST00000439388.5:c.713C=	ENSP00000403084.1:p.Thr238=
ENST00000616662.4:c.713C=	ENSP00000484683.1:p.Thr238=
NM_001134707.1:c.713C=	NP_001128179.1:p.Thr238=
NM_007101.3:c.713C=	NP_009032.2:p.Thr238=
XM_006716990.2:c.713C=	XP_006717053.1:p.Thr238=
XM_011518333.1:c.713C=	XP_011516635.1:p.Thr238=
XR_929726.1:n.880C=
XR_929727.1:n.880C=
XR_929728.1:n.880C=
XM_017014367.1:c.713C=	XP_016869856.1:p.Thr238=
XM_017014368.1:c.713C=	XP_016869857.1:p.Thr238=
XR_001746213.1:n.1009C=
XR_001746214.1:n.2192C=
XR_001746215.1:n.1011C=
XR_001746216.1:n.1009C=
XR_001746217.1:n.1009C=
XR_001746218.1:n.1009C=
XR_929726.2:n.880C=
NM_001134707.2:c.713C= MANE Select	NP_001128179.1:p.Thr238=
NM_007101.4:c.713C=	NP_009032.2:p.Thr238=