Canonical Allele Identifier: CA3202881

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 3021252
• ClinVar RCV Id: RCV003872395
• dbSNP Id: rs756343680
• ExAC: 5:13793672 T / C
• gnomAD v2: 5-13793672-T-C
• gnomAD v4: 5-13793563-T-C
• MyVariant Identifiers: chr5:g.13793672T>C (hg19) ; chr5:g.13793563T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793563T>C , CM000667.2:g.13793563T>C	GRCh38
NC_000005.9:g.13793672T>C , CM000667.1:g.13793672T>C	GRCh37
NC_000005.8:g.13846672T>C	NCBI36
NG_013081.1:g.155918A>G
NG_013081.2:g.155918A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8176A>G MANE Select	ENSP00000265104.4:p.Ile2726Val
ENST00000681290.1:c.8131A>G	ENSP00000505288.1:p.Ile2711Val
ENST00000265104.4:c.8176A>G	ENSP00000265104.4:p.Ile2726Val
NM_001369.2:c.8176A>G	NP_001360.1:p.Ile2726Val
XM_005248262.2:c.8131A>G	XP_005248319.1:p.Ile2711Val
XM_011513990.1:c.8176A>G	XP_011512292.1:p.Ile2726Val
XR_925598.1:n.8383A>G
XM_005248262.3:c.8284A>G	XP_005248319.2:p.Ile2762Val
XM_017009177.1:c.8284A>G	XP_016864666.1:p.Ile2762Val
XM_017009178.1:c.7189A>G	XP_016864667.1:p.Ile2397Val
XM_017009179.2:c.7189A>G	XP_016864668.1:p.Ile2397Val
XM_017009180.1:c.8284A>G	XP_016864669.1:p.Ile2762Val
XM_017009181.1:c.8284A>G	XP_016864670.1:p.Ile2762Val
XM_017009182.1:c.8284A>G	XP_016864671.1:p.Ile2762Val
XM_017009183.1:c.8284A>G	XP_016864672.1:p.Ile2762Val
XM_017009184.1:c.8284A>G	XP_016864673.1:p.Ile2762Val
XM_017009185.1:c.3373A>G	XP_016864674.1:p.Ile1125Val
XM_017009186.1:c.2926A>G	XP_016864675.1:p.Ile976Val
XM_017009188.1:c.2263A>G	XP_016864677.1:p.Ile755Val
XM_024454388.1:c.7189A>G	XP_024310156.1:p.Ile2397Val
XM_024454389.1:c.6778A>G	XP_024310157.1:p.Ile2260Val
XR_001742034.1:n.8301A>G
XR_001742035.1:n.8301A>G
NM_001369.3:c.8176A>G MANE Select	NP_001360.1:p.Ile2726Val