Canonical Allele Identifier: CA1528440748

Gene: DNAH5

Linked Data

• dbSNP Id: rs1757012587

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13791682T>A , CM000667.2:g.13791682T>A	GRCh38
NC_000005.9:g.13791791T>A , CM000667.1:g.13791791T>A	GRCh37
NC_000005.8:g.13844791T>A	NCBI36
NG_013081.1:g.157799A>T
NG_013081.2:g.157799A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8448+312A>T MANE Select	ENSP00000265104.4:n.8448+312A>T
ENST00000681290.1:c.8403+312A>T	ENSP00000505288.1:n.8403+312A>T
ENST00000265104.4:c.8448+312A>T	ENSP00000265104.4:n.8448+312A>T
NM_001369.2:c.8448+312A>T	NP_001360.1:n.8448+312A>T
XM_005248262.2:c.8403+312A>T	XP_005248319.1:n.8403+312A>T
XM_011513990.1:c.8448+312A>T	XP_011512292.1:n.8448+312A>T
XR_925598.1:n.8655+312A>T
XM_005248262.3:c.8556+312A>T	XP_005248319.2:n.8556+312A>T
XM_017009177.1:c.8556+312A>T	XP_016864666.1:n.8556+312A>T
XM_017009178.1:c.7461+312A>T	XP_016864667.1:n.7461+312A>T
XM_017009179.2:c.7461+312A>T	XP_016864668.1:n.7461+312A>T
XM_017009180.1:c.8556+312A>T	XP_016864669.1:n.8556+312A>T
XM_017009181.1:c.8556+312A>T	XP_016864670.1:n.8556+312A>T
XM_017009182.1:c.8556+312A>T	XP_016864671.1:n.8556+312A>T
XM_017009183.1:c.8556+312A>T	XP_016864672.1:n.8556+312A>T
XM_017009184.1:c.8556+312A>T	XP_016864673.1:n.8556+312A>T
XM_017009185.1:c.3645+312A>T	XP_016864674.1:n.3645+312A>T
XM_017009186.1:c.3198+312A>T	XP_016864675.1:n.3198+312A>T
XM_017009188.1:c.2535+312A>T	XP_016864677.1:n.2535+312A>T
XM_024454388.1:c.7461+312A>T	XP_024310156.1:n.7461+312A>T
XM_024454389.1:c.7050+312A>T	XP_024310157.1:n.7050+312A>T
XR_001742034.1:n.8573+312A>T
XR_001742035.1:n.8573+312A>T
NM_001369.3:c.8448+312A>T MANE Select	NP_001360.1:n.8448+312A>T