Canonical Allele Identifier: CA2673268009

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13735707-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735713dup , CM000667.2:g.13735713dup	GRCh38
NC_000005.9:g.13735822dup , CM000667.1:g.13735822dup	GRCh37
NC_000005.8:g.13788822dup	NCBI36
NG_013081.1:g.213773dup
NG_013081.2:g.213773dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.11570+110dup MANE Select	ENSP00000265104.4:n.11570+110dup
ENST00000681290.1:c.11525+110dup	ENSP00000505288.1:n.11525+110dup
ENST00000265104.4:c.11570+110dup	ENSP00000265104.4:n.11570+110dup
NM_001369.2:c.11570+110dup	NP_001360.1:n.11570+110dup
XM_005248262.2:c.11525+110dup	XP_005248319.1:n.11525+110dup
XM_005248262.3:c.11678+110dup	XP_005248319.2:n.11678+110dup
XM_017009177.1:c.11678+110dup	XP_016864666.1:n.11678+110dup
XM_017009178.1:c.10583+110dup	XP_016864667.1:n.10583+110dup
XM_017009179.2:c.10583+110dup	XP_016864668.1:n.10583+110dup
XM_017009180.1:c.11678+110dup	XP_016864669.1:n.11678+110dup
XM_017009181.1:c.11678+110dup	XP_016864670.1:n.11678+110dup
XM_017009182.1:c.*4+110dup	XP_016864671.1:n.*4+110dup
XM_017009185.1:c.6767+110dup	XP_016864674.1:n.6767+110dup
XM_017009186.1:c.6320+110dup	XP_016864675.1:n.6320+110dup
XM_017009188.1:c.5657+110dup	XP_016864677.1:n.5657+110dup
XM_024454388.1:c.10583+110dup	XP_024310156.1:n.10583+110dup
XM_024454389.1:c.10172+110dup	XP_024310157.1:n.10172+110dup
NM_001369.3:c.11570+110dup MANE Select	NP_001360.1:n.11570+110dup