Canonical Allele Identifier: CA359212996

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13781068T>C (hg19) ; chr5:g.13780959T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13780959T>C , CM000667.2:g.13780959T>C	GRCh38
NC_000005.9:g.13781068T>C , CM000667.1:g.13781068T>C	GRCh37
NC_000005.8:g.13834068T>C	NCBI36
NG_013081.1:g.168522A>G
NG_013081.2:g.168522A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8821A>G MANE Select	ENSP00000265104.4:p.Ile2941Val
ENST00000681290.1:c.8776A>G	ENSP00000505288.1:p.Ile2926Val
ENST00000265104.4:c.8821A>G	ENSP00000265104.4:p.Ile2941Val
NM_001369.2:c.8821A>G	NP_001360.1:p.Ile2941Val
XM_005248262.2:c.8776A>G	XP_005248319.1:p.Ile2926Val
XM_011513990.1:c.8821A>G	XP_011512292.1:p.Ile2941Val
XR_925598.1:n.9028-3604A>G
XM_005248262.3:c.8929A>G	XP_005248319.2:p.Ile2977Val
XM_017009177.1:c.8929A>G	XP_016864666.1:p.Ile2977Val
XM_017009178.1:c.7834A>G	XP_016864667.1:p.Ile2612Val
XM_017009179.2:c.7834A>G	XP_016864668.1:p.Ile2612Val
XM_017009180.1:c.8929A>G	XP_016864669.1:p.Ile2977Val
XM_017009181.1:c.8929A>G	XP_016864670.1:p.Ile2977Val
XM_017009182.1:c.8929A>G	XP_016864671.1:p.Ile2977Val
XM_017009183.1:c.8929A>G	XP_016864672.1:p.Ile2977Val
XM_017009184.1:c.8929A>G	XP_016864673.1:p.Ile2977Val
XM_017009185.1:c.4018A>G	XP_016864674.1:p.Ile1340Val
XM_017009186.1:c.3571A>G	XP_016864675.1:p.Ile1191Val
XM_017009188.1:c.2908A>G	XP_016864677.1:p.Ile970Val
XM_024454388.1:c.7834A>G	XP_024310156.1:p.Ile2612Val
XM_024454389.1:c.7423A>G	XP_024310157.1:p.Ile2475Val
XR_001742034.1:n.8946-3604A>G
XR_001742035.1:n.8946-3604A>G
NM_001369.3:c.8821A>G MANE Select	NP_001360.1:p.Ile2941Val