Canonical Allele Identifier: CA467620293

Gene: SARDH

Linked Data

• gnomAD v4: 9-133729828-G-A
• MyVariant Identifiers: chr9:g.136594950G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133729828G>A , CM000671.2:g.133729828G>A	GRCh38
NC_000009.11:g.136594950G>A , CM000671.1:g.136594950G>A	GRCh37
NC_000009.10:g.135584771G>A	NCBI36
NG_008987.1:g.15128C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000439388.6:c.852C>T MANE Select	ENSP00000403084.1:p.Val284=
ENST00000298628.6:c.852C>T	ENSP00000298628.5:p.Val284=
ENST00000371867.5:c.585C>T	ENSP00000360933.1:p.Val195=
ENST00000371872.8:c.852C>T	ENSP00000360938.4:p.Val284=
ENST00000422262.6:c.12C>T	ENSP00000415537.3:p.Val4=
ENST00000427237.6:c.852C>T	ENSP00000394210.2:p.Val284=
ENST00000439388.5:c.852C>T	ENSP00000403084.1:p.Val284=
ENST00000616662.4:c.852C>T	ENSP00000484683.1:p.Val284=
NM_001134707.1:c.852C>T	NP_001128179.1:p.Val284=
NM_007101.3:c.852C>T	NP_009032.2:p.Val284=
XM_006716990.2:c.852C>T	XP_006717053.1:p.Val284=
XM_011518333.1:c.852C>T	XP_011516635.1:p.Val284=
XR_929726.1:n.1019C>T
XR_929727.1:n.1019C>T
XR_929728.1:n.1019C>T
XM_017014367.1:c.852C>T	XP_016869856.1:p.Val284=
XM_017014368.1:c.852C>T	XP_016869857.1:p.Val284=
XR_001746213.1:n.1148C>T
XR_001746214.1:n.2331C>T
XR_001746215.1:n.1150C>T
XR_001746216.1:n.1148C>T
XR_001746217.1:n.1148C>T
XR_001746218.1:n.1148C>T
XR_929726.2:n.1019C>T
NM_001134707.2:c.852C>T MANE Select	NP_001128179.1:p.Val284=
NM_007101.4:c.852C>T	NP_009032.2:p.Val284=