Canonical Allele Identifier: CA467630025

Gene: SARDH

Linked Data

• MyVariant Identifiers: chr9:g.136536718A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133671596A>G , CM000671.2:g.133671596A>G	GRCh38
NC_000009.11:g.136536718A>G , CM000671.1:g.136536718A>G	GRCh37
NC_000009.10:g.135526539A>G	NCBI36
NG_008987.1:g.73360T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439388.6:c.2265T>C MANE Select	ENSP00000403084.1:p.Gly755=
ENST00000371868.5:c.549T>C	ENSP00000360934.1:p.Gly183=
ENST00000371872.8:c.2265T>C	ENSP00000360938.4:p.Gly755=
ENST00000422262.6:c.1425T>C	ENSP00000415537.3:p.Gly475=
ENST00000439388.5:c.2265T>C	ENSP00000403084.1:p.Gly755=
NM_001134707.1:c.2265T>C	NP_001128179.1:p.Gly755=
NM_007101.3:c.2265T>C	NP_009032.2:p.Gly755=
XM_006716990.2:c.2265T>C	XP_006717053.1:p.Gly755=
XM_011518333.1:c.2265T>C	XP_011516635.1:p.Gly755=
XR_929726.1:n.2432T>C
XR_929727.1:n.2432T>C
XR_929728.1:n.2432T>C
XM_017014367.1:c.2265T>C	XP_016869856.1:p.Gly755=
XM_017014368.1:c.2265T>C	XP_016869857.1:p.Gly755=
XR_001746213.1:n.2561T>C
XR_001746214.1:n.3744T>C
XR_001746215.1:n.2563T>C
XR_001746216.1:n.2561T>C
XR_001746217.1:n.2561T>C
XR_001746218.1:n.2413T>C
XR_002956762.1:n.2517T>C
XR_929726.2:n.2432T>C
NM_001134707.2:c.2265T>C MANE Select	NP_001128179.1:p.Gly755=
NM_007101.4:c.2265T>C	NP_009032.2:p.Gly755=