Canonical Allele Identifier: CA1528458676

Gene: DNAH5

Linked Data

• dbSNP Id: rs1763509411
• gnomAD v4: 5-13830459-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13830460dup , CM000667.2:g.13830460dup	GRCh38
NC_000005.9:g.13830569dup , CM000667.1:g.13830569dup	GRCh37
NC_000005.8:g.13883569dup	NCBI36
NG_013081.1:g.119021dup
NG_013081.2:g.119021dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683090.1:n.992+137dup
ENST00000265104.5:c.6061+137dup MANE Select	ENSP00000265104.4:n.6061+137dup
ENST00000681290.1:c.6016+137dup	ENSP00000505288.1:n.6016+137dup
ENST00000265104.4:c.6061+137dup	ENSP00000265104.4:n.6061+137dup
NM_001369.2:c.6061+137dup	NP_001360.1:n.6061+137dup
XM_005248262.2:c.6016+137dup	XP_005248319.1:n.6016+137dup
XM_011513990.1:c.6061+137dup	XP_011512292.1:n.6061+137dup
XR_925598.1:n.6268+137dup
XM_005248262.3:c.6169+137dup	XP_005248319.2:n.6169+137dup
XM_017009177.1:c.6169+137dup	XP_016864666.1:n.6169+137dup
XM_017009178.1:c.5074+137dup	XP_016864667.1:n.5074+137dup
XM_017009179.2:c.5074+137dup	XP_016864668.1:n.5074+137dup
XM_017009180.1:c.6169+137dup	XP_016864669.1:n.6169+137dup
XM_017009181.1:c.6169+137dup	XP_016864670.1:n.6169+137dup
XM_017009182.1:c.6169+137dup	XP_016864671.1:n.6169+137dup
XM_017009183.1:c.6169+137dup	XP_016864672.1:n.6169+137dup
XM_017009184.1:c.6169+137dup	XP_016864673.1:n.6169+137dup
XM_017009185.1:c.1258+137dup	XP_016864674.1:n.1258+137dup
XM_017009186.1:c.811+137dup	XP_016864675.1:n.811+137dup
XM_017009187.1:c.6169+137dup	XP_016864676.1:n.6169+137dup
XM_017009188.1:c.148+137dup	XP_016864677.1:n.148+137dup
XM_024454388.1:c.5074+137dup	XP_024310156.1:n.5074+137dup
XM_024454389.1:c.4663+137dup	XP_024310157.1:n.4663+137dup
XR_001742034.1:n.6186+137dup
XR_001742035.1:n.6186+137dup
NM_001369.3:c.6061+137dup MANE Select	NP_001360.1:n.6061+137dup