Canonical Allele Identifier: CA2673271049

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13791957-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13791957C>T , CM000667.2:g.13791957C>T	GRCh38
NC_000005.9:g.13792066C>T , CM000667.1:g.13792066C>T	GRCh37
NC_000005.8:g.13845066C>T	NCBI36
NG_013081.1:g.157524G>A
NG_013081.2:g.157524G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.8448+37G>A MANE Select	ENSP00000265104.4:n.8448+37G>A
ENST00000681290.1:c.8403+37G>A	ENSP00000505288.1:n.8403+37G>A
ENST00000265104.4:c.8448+37G>A	ENSP00000265104.4:n.8448+37G>A
NM_001369.2:c.8448+37G>A	NP_001360.1:n.8448+37G>A
XM_005248262.2:c.8403+37G>A	XP_005248319.1:n.8403+37G>A
XM_011513990.1:c.8448+37G>A	XP_011512292.1:n.8448+37G>A
XR_925598.1:n.8655+37G>A
XM_005248262.3:c.8556+37G>A	XP_005248319.2:n.8556+37G>A
XM_017009177.1:c.8556+37G>A	XP_016864666.1:n.8556+37G>A
XM_017009178.1:c.7461+37G>A	XP_016864667.1:n.7461+37G>A
XM_017009179.2:c.7461+37G>A	XP_016864668.1:n.7461+37G>A
XM_017009180.1:c.8556+37G>A	XP_016864669.1:n.8556+37G>A
XM_017009181.1:c.8556+37G>A	XP_016864670.1:n.8556+37G>A
XM_017009182.1:c.8556+37G>A	XP_016864671.1:n.8556+37G>A
XM_017009183.1:c.8556+37G>A	XP_016864672.1:n.8556+37G>A
XM_017009184.1:c.8556+37G>A	XP_016864673.1:n.8556+37G>A
XM_017009185.1:c.3645+37G>A	XP_016864674.1:n.3645+37G>A
XM_017009186.1:c.3198+37G>A	XP_016864675.1:n.3198+37G>A
XM_017009188.1:c.2535+37G>A	XP_016864677.1:n.2535+37G>A
XM_024454388.1:c.7461+37G>A	XP_024310156.1:n.7461+37G>A
XM_024454389.1:c.7050+37G>A	XP_024310157.1:n.7050+37G>A
XR_001742034.1:n.8573+37G>A
XR_001742035.1:n.8573+37G>A
NM_001369.3:c.8448+37G>A MANE Select	NP_001360.1:n.8448+37G>A