Canonical Allele Identifier: CA10620181

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 350903
• ClinVar RCV Id: RCV000391231
• dbSNP Id: rs574438524
• gnomAD v2: 5-13690587-C-T
• gnomAD v3: 5-13690478-C-T
• gnomAD v4: 5-13690478-C-T
• MyVariant Identifiers: chr5:g.13690587C>T (hg19) ; chr5:g.13690478C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13690478C>T , CM000667.2:g.13690478C>T	GRCh38
NC_000005.9:g.13690587C>T , CM000667.1:g.13690587C>T	GRCh37
NC_000005.8:g.13743587C>T	NCBI36
NG_013081.1:g.259003G>A
NG_013081.2:g.259003G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.2714G>A
ENST00000265104.5:c.*1506G>A MANE Select	ENSP00000265104.4:n.*1506G>A
ENST00000681290.1:c.*1506G>A	ENSP00000505288.1:n.*1506G>A
ENST00000265104.4:c.*1506G>A	ENSP00000265104.4:n.*1506G>A
NM_001369.2:c.*1506G>A	NP_001360.1:n.*1506G>A
XM_005248262.2:c.*1506G>A	XP_005248319.1:n.*1506G>A
XM_005248262.3:c.*1506G>A	XP_005248319.2:n.*1506G>A
XM_017009177.1:c.*1506G>A	XP_016864666.1:n.*1506G>A
XM_017009178.1:c.*1506G>A	XP_016864667.1:n.*1506G>A
XM_017009179.2:c.*1506G>A	XP_016864668.1:n.*1506G>A
XM_017009185.1:c.*1506G>A	XP_016864674.1:n.*1506G>A
XM_017009186.1:c.*1506G>A	XP_016864675.1:n.*1506G>A
XM_017009188.1:c.*1506G>A	XP_016864677.1:n.*1506G>A
XM_024454388.1:c.*1506G>A	XP_024310156.1:n.*1506G>A
XM_024454389.1:c.*1506G>A	XP_024310157.1:n.*1506G>A
NM_001369.3:c.*1506G>A MANE Select	NP_001360.1:n.*1506G>A