Canonical Allele Identifier: CA375426781

Gene: SARDH

Linked Data

• MyVariant Identifiers: chr9:g.136595288T>C (hg19) ; chr9:g.133730166T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133730166T>C , CM000671.2:g.133730166T>C	GRCh38
NC_000009.11:g.136595288T>C , CM000671.1:g.136595288T>C	GRCh37
NC_000009.10:g.135585109T>C	NCBI36
NG_008987.1:g.14790A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439388.6:c.712A>G MANE Select	ENSP00000403084.1:p.Thr238Ala
ENST00000298628.6:c.712A>G	ENSP00000298628.5:p.Thr238Ala
ENST00000371867.5:c.445A>G	ENSP00000360933.1:p.Thr149Ala
ENST00000371872.8:c.712A>G	ENSP00000360938.4:p.Thr238Ala
ENST00000427237.6:c.712A>G	ENSP00000394210.2:p.Thr238Ala
ENST00000439388.5:c.712A>G	ENSP00000403084.1:p.Thr238Ala
ENST00000616662.4:c.712A>G	ENSP00000484683.1:p.Thr238Ala
NM_001134707.1:c.712A>G	NP_001128179.1:p.Thr238Ala
NM_007101.3:c.712A>G	NP_009032.2:p.Thr238Ala
XM_006716990.2:c.712A>G	XP_006717053.1:p.Thr238Ala
XM_011518333.1:c.712A>G	XP_011516635.1:p.Thr238Ala
XR_929726.1:n.879A>G
XR_929727.1:n.879A>G
XR_929728.1:n.879A>G
XM_017014367.1:c.712A>G	XP_016869856.1:p.Thr238Ala
XM_017014368.1:c.712A>G	XP_016869857.1:p.Thr238Ala
XR_001746213.1:n.1008A>G
XR_001746214.1:n.2191A>G
XR_001746215.1:n.1010A>G
XR_001746216.1:n.1008A>G
XR_001746217.1:n.1008A>G
XR_001746218.1:n.1008A>G
XR_929726.2:n.879A>G
NM_001134707.2:c.712A>G MANE Select	NP_001128179.1:p.Thr238Ala
NM_007101.4:c.712A>G	NP_009032.2:p.Thr238Ala