Canonical Allele Identifier: CA5314698

Gene: SARDH

Linked Data

• dbSNP Id: rs772942604
• ExAC: 9:136595328 G / T
• gnomAD v2: 9-136595328-G-T
• gnomAD v3: 9-133730206-G-T
• gnomAD v4: 9-133730206-G-T
• MyVariant Identifiers: chr9:g.136595328G>T (hg19) ; chr9:g.133730206G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133730206G>T , CM000671.2:g.133730206G>T	GRCh38
NC_000009.11:g.136595328G>T , CM000671.1:g.136595328G>T	GRCh37
NC_000009.10:g.135585149G>T	NCBI36
NG_008987.1:g.14750C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439388.6:c.691-19C>A MANE Select	ENSP00000403084.1:n.691-19C>A
ENST00000298628.6:c.691-19C>A	ENSP00000298628.5:n.691-19C>A
ENST00000371867.5:c.424-19C>A	ENSP00000360933.1:n.424-19C>A
ENST00000371872.8:c.691-19C>A	ENSP00000360938.4:n.691-19C>A
ENST00000427237.6:c.691-19C>A	ENSP00000394210.2:n.691-19C>A
ENST00000439388.5:c.691-19C>A	ENSP00000403084.1:n.691-19C>A
ENST00000616662.4:c.691-19C>A	ENSP00000484683.1:n.691-19C>A
NM_001134707.1:c.691-19C>A	NP_001128179.1:n.691-19C>A
NM_007101.3:c.691-19C>A	NP_009032.2:n.691-19C>A
XM_006716990.2:c.691-19C>A	XP_006717053.1:n.691-19C>A
XM_011518333.1:c.691-19C>A	XP_011516635.1:n.691-19C>A
XR_929726.1:n.858-19C>A
XR_929727.1:n.858-19C>A
XR_929728.1:n.858-19C>A
XM_017014367.1:c.691-19C>A	XP_016869856.1:n.691-19C>A
XM_017014368.1:c.691-19C>A	XP_016869857.1:n.691-19C>A
XR_001746213.1:n.987-19C>A
XR_001746214.1:n.2170-19C>A
XR_001746215.1:n.989-19C>A
XR_001746216.1:n.987-19C>A
XR_001746217.1:n.987-19C>A
XR_001746218.1:n.987-19C>A
XR_929726.2:n.858-19C>A
NM_001134707.2:c.691-19C>A MANE Select	NP_001128179.1:n.691-19C>A
NM_007101.4:c.691-19C>A	NP_009032.2:n.691-19C>A