Canonical Allele Identifier: CA3204204

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 454769
• ClinVar RCV Id: RCV000527499 ; RCV003338643 ; RCV003431069
• dbSNP Id: rs73055857
• ExAC: 5:13871054 C / T
• gnomAD v2: 5-13871054-C-T
• gnomAD v3: 5-13870945-C-T
• gnomAD v4: 5-13870945-C-T
• MyVariant Identifiers: chr5:g.13871054C>T (hg19) ; chr5:g.13870945C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13870945C>T , CM000667.2:g.13870945C>T	GRCh38
NC_000005.9:g.13871054C>T , CM000667.1:g.13871054C>T	GRCh37
NC_000005.8:g.13924054C>T	NCBI36
NG_013081.1:g.78536G>A
NG_013081.2:g.78536G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.3656G>A MANE Select	ENSP00000265104.4:p.Arg1219His
ENST00000681290.1:c.3611G>A	ENSP00000505288.1:p.Arg1204His
ENST00000265104.4:c.3656G>A	ENSP00000265104.4:p.Arg1219His
NM_001369.2:c.3656G>A	NP_001360.1:p.Arg1219His
XM_005248262.2:c.3611G>A	XP_005248319.1:p.Arg1204His
XM_011513990.1:c.3656G>A	XP_011512292.1:p.Arg1219His
XR_925598.1:n.3863G>A
XM_005248262.3:c.3764G>A	XP_005248319.2:p.Arg1255His
XM_017009177.1:c.3764G>A	XP_016864666.1:p.Arg1255His
XM_017009178.1:c.2669G>A	XP_016864667.1:p.Arg890His
XM_017009179.2:c.2669G>A	XP_016864668.1:p.Arg890His
XM_017009180.1:c.3764G>A	XP_016864669.1:p.Arg1255His
XM_017009181.1:c.3764G>A	XP_016864670.1:p.Arg1255His
XM_017009182.1:c.3764G>A	XP_016864671.1:p.Arg1255His
XM_017009183.1:c.3764G>A	XP_016864672.1:p.Arg1255His
XM_017009184.1:c.3764G>A	XP_016864673.1:p.Arg1255His
XM_017009187.1:c.3764G>A	XP_016864676.1:p.Arg1255His
XM_024454388.1:c.2669G>A	XP_024310156.1:p.Arg890His
XM_024454389.1:c.2258G>A	XP_024310157.1:p.Arg753His
XR_001742034.1:n.3781G>A
XR_001742035.1:n.3781G>A
NM_001369.3:c.3656G>A MANE Select	NP_001360.1:p.Arg1219His