Canonical Allele Identifier: CA467620308

Gene: SARDH

Linked Data

• MyVariant Identifiers: chr9:g.136594953T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133729831T>G , CM000671.2:g.133729831T>G	GRCh38
NC_000009.11:g.136594953T>G , CM000671.1:g.136594953T>G	GRCh37
NC_000009.10:g.135584774T>G	NCBI36
NG_008987.1:g.15125A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000439388.6:c.849A>C MANE Select	ENSP00000403084.1:p.Gly283=
ENST00000298628.6:c.849A>C	ENSP00000298628.5:p.Gly283=
ENST00000371867.5:c.582A>C	ENSP00000360933.1:p.Gly194=
ENST00000371872.8:c.849A>C	ENSP00000360938.4:p.Gly283=
ENST00000422262.6:c.9A>C	ENSP00000415537.3:p.Gly3=
ENST00000427237.6:c.849A>C	ENSP00000394210.2:p.Gly283=
ENST00000439388.5:c.849A>C	ENSP00000403084.1:p.Gly283=
ENST00000616662.4:c.849A>C	ENSP00000484683.1:p.Gly283=
NM_001134707.1:c.849A>C	NP_001128179.1:p.Gly283=
NM_007101.3:c.849A>C	NP_009032.2:p.Gly283=
XM_006716990.2:c.849A>C	XP_006717053.1:p.Gly283=
XM_011518333.1:c.849A>C	XP_011516635.1:p.Gly283=
XR_929726.1:n.1016A>C
XR_929727.1:n.1016A>C
XR_929728.1:n.1016A>C
XM_017014367.1:c.849A>C	XP_016869856.1:p.Gly283=
XM_017014368.1:c.849A>C	XP_016869857.1:p.Gly283=
XR_001746213.1:n.1145A>C
XR_001746214.1:n.2328A>C
XR_001746215.1:n.1147A>C
XR_001746216.1:n.1145A>C
XR_001746217.1:n.1145A>C
XR_001746218.1:n.1145A>C
XR_929726.2:n.1016A>C
NM_001134707.2:c.849A>C MANE Select	NP_001128179.1:p.Gly283=
NM_007101.4:c.849A>C	NP_009032.2:p.Gly283=