Canonical Allele Identifier: CA1528463560

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841580_13841581delinsTA , CM000667.2:g.13841580_13841581delinsTA	GRCh38
NC_000005.9:g.13841689_13841690delinsTA , CM000667.1:g.13841689_13841690delinsTA	GRCh37
NC_000005.8:g.13894689_13894690delinsTA	NCBI36
NG_013081.1:g.107900_107901delinsTA
NG_013081.2:g.107900_107901delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5484+111_5484+112delinsTA MANE Select	ENSP00000265104.4:n.5484+111_5484+112delinsTA
ENST00000681290.1:c.5439+111_5439+112delinsTA	ENSP00000505288.1:n.5439+111_5439+112delinsTA
ENST00000265104.4:c.5484+111_5484+112delinsTA	ENSP00000265104.4:n.5484+111_5484+112delinsTA
NM_001369.2:c.5484+111_5484+112delinsTA	NP_001360.1:n.5484+111_5484+112delinsTA
XM_005248262.2:c.5439+111_5439+112delinsTA	XP_005248319.1:n.5439+111_5439+112delinsTA
XM_011513990.1:c.5484+111_5484+112delinsTA	XP_011512292.1:n.5484+111_5484+112delinsTA
XR_925598.1:n.5691+111_5691+112delinsTA
XM_005248262.3:c.5592+111_5592+112delinsTA	XP_005248319.2:n.5592+111_5592+112delinsTA
XM_017009177.1:c.5592+111_5592+112delinsTA	XP_016864666.1:n.5592+111_5592+112delinsTA
XM_017009178.1:c.4497+111_4497+112delinsTA	XP_016864667.1:n.4497+111_4497+112delinsTA
XM_017009179.2:c.4497+111_4497+112delinsTA	XP_016864668.1:n.4497+111_4497+112delinsTA
XM_017009180.1:c.5592+111_5592+112delinsTA	XP_016864669.1:n.5592+111_5592+112delinsTA
XM_017009181.1:c.5592+111_5592+112delinsTA	XP_016864670.1:n.5592+111_5592+112delinsTA
XM_017009182.1:c.5592+111_5592+112delinsTA	XP_016864671.1:n.5592+111_5592+112delinsTA
XM_017009183.1:c.5592+111_5592+112delinsTA	XP_016864672.1:n.5592+111_5592+112delinsTA
XM_017009184.1:c.5592+111_5592+112delinsTA	XP_016864673.1:n.5592+111_5592+112delinsTA
XM_017009185.1:c.681+111_681+112delinsTA	XP_016864674.1:n.681+111_681+112delinsTA
XM_017009186.1:c.234+111_234+112delinsTA	XP_016864675.1:n.234+111_234+112delinsTA
XM_017009187.1:c.5592+111_5592+112delinsTA	XP_016864676.1:n.5592+111_5592+112delinsTA
XM_024454388.1:c.4497+111_4497+112delinsTA	XP_024310156.1:n.4497+111_4497+112delinsTA
XM_024454389.1:c.4086+111_4086+112delinsTA	XP_024310157.1:n.4086+111_4086+112delinsTA
XR_001742034.1:n.5609+111_5609+112delinsTA
XR_001742035.1:n.5609+111_5609+112delinsTA
NM_001369.3:c.5484+111_5484+112delinsTA MANE Select	NP_001360.1:n.5484+111_5484+112delinsTA