Canonical Allele Identifier: CA2692402574

Gene: SARDH

Linked Data

• gnomAD v4: 9-133730245-ACCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133730247_133730249del , CM000671.2:g.133730247_133730249del	GRCh38
NC_000009.11:g.136595369_136595371del , CM000671.1:g.136595369_136595371del	GRCh37
NC_000009.10:g.135585190_135585192del	NCBI36
NG_008987.1:g.14708_14710del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439388.6:c.691-61_691-59del MANE Select	ENSP00000403084.1:n.691-61_691-59del
ENST00000298628.6:c.691-61_691-59del	ENSP00000298628.5:n.691-61_691-59del
ENST00000371867.5:c.424-61_424-59del	ENSP00000360933.1:n.424-61_424-59del
ENST00000371872.8:c.691-61_691-59del	ENSP00000360938.4:n.691-61_691-59del
ENST00000427237.6:c.691-61_691-59del	ENSP00000394210.2:n.691-61_691-59del
ENST00000439388.5:c.691-61_691-59del	ENSP00000403084.1:n.691-61_691-59del
ENST00000616662.4:c.691-61_691-59del	ENSP00000484683.1:n.691-61_691-59del
NM_001134707.1:c.691-61_691-59del	NP_001128179.1:n.691-61_691-59del
NM_007101.3:c.691-61_691-59del	NP_009032.2:n.691-61_691-59del
XM_006716990.2:c.691-61_691-59del	XP_006717053.1:n.691-61_691-59del
XM_011518333.1:c.691-61_691-59del	XP_011516635.1:n.691-61_691-59del
XR_929726.1:n.858-61_858-59del
XR_929727.1:n.858-61_858-59del
XR_929728.1:n.858-61_858-59del
XM_017014367.1:c.691-61_691-59del	XP_016869856.1:n.691-61_691-59del
XM_017014368.1:c.691-61_691-59del	XP_016869857.1:n.691-61_691-59del
XR_001746213.1:n.987-61_987-59del
XR_001746214.1:n.2170-61_2170-59del
XR_001746215.1:n.989-61_989-59del
XR_001746216.1:n.987-61_987-59del
XR_001746217.1:n.987-61_987-59del
XR_001746218.1:n.987-61_987-59del
XR_929726.2:n.858-61_858-59del
NM_001134707.2:c.691-61_691-59del MANE Select	NP_001128179.1:n.691-61_691-59del
NM_007101.4:c.691-61_691-59del	NP_009032.2:n.691-61_691-59del