Canonical Allele Identifier: CA359221834

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13794065T>A (hg19) ; chr5:g.13793956T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793956T>A , CM000667.2:g.13793956T>A	GRCh38
NC_000005.9:g.13794065T>A , CM000667.1:g.13794065T>A	GRCh37
NC_000005.8:g.13847065T>A	NCBI36
NG_013081.1:g.155525A>T
NG_013081.2:g.155525A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.7990A>T MANE Select	ENSP00000265104.4:p.Ile2664Phe
ENST00000681290.1:c.7945A>T	ENSP00000505288.1:p.Ile2649Phe
ENST00000265104.4:c.7990A>T	ENSP00000265104.4:p.Ile2664Phe
NM_001369.2:c.7990A>T	NP_001360.1:p.Ile2664Phe
XM_005248262.2:c.7945A>T	XP_005248319.1:p.Ile2649Phe
XM_011513990.1:c.7990A>T	XP_011512292.1:p.Ile2664Phe
XR_925598.1:n.8197A>T
XM_005248262.3:c.8098A>T	XP_005248319.2:p.Ile2700Phe
XM_017009177.1:c.8098A>T	XP_016864666.1:p.Ile2700Phe
XM_017009178.1:c.7003A>T	XP_016864667.1:p.Ile2335Phe
XM_017009179.2:c.7003A>T	XP_016864668.1:p.Ile2335Phe
XM_017009180.1:c.8098A>T	XP_016864669.1:p.Ile2700Phe
XM_017009181.1:c.8098A>T	XP_016864670.1:p.Ile2700Phe
XM_017009182.1:c.8098A>T	XP_016864671.1:p.Ile2700Phe
XM_017009183.1:c.8098A>T	XP_016864672.1:p.Ile2700Phe
XM_017009184.1:c.8098A>T	XP_016864673.1:p.Ile2700Phe
XM_017009185.1:c.3187A>T	XP_016864674.1:p.Ile1063Phe
XM_017009186.1:c.2740A>T	XP_016864675.1:p.Ile914Phe
XM_017009188.1:c.2077A>T	XP_016864677.1:p.Ile693Phe
XM_024454388.1:c.7003A>T	XP_024310156.1:p.Ile2335Phe
XM_024454389.1:c.6592A>T	XP_024310157.1:p.Ile2198Phe
XR_001742034.1:n.8115A>T
XR_001742035.1:n.8115A>T
NM_001369.3:c.7990A>T MANE Select	NP_001360.1:p.Ile2664Phe