Canonical Allele Identifier: CA1528458243

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841601_13841603delinsTTA , CM000667.2:g.13841601_13841603delinsTTA	GRCh38
NC_000005.9:g.13841710_13841712delinsTTA , CM000667.1:g.13841710_13841712delinsTTA	GRCh37
NC_000005.8:g.13894710_13894712delinsTTA	NCBI36
NG_013081.1:g.107878_107880delinsTAA
NG_013081.2:g.107878_107880delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5484+89_5484+91delinsTAA MANE Select	ENSP00000265104.4:n.5484+89_5484+91delinsTAA
ENST00000681290.1:c.5439+89_5439+91delinsTAA	ENSP00000505288.1:n.5439+89_5439+91delinsTAA
ENST00000265104.4:c.5484+89_5484+91delinsTAA	ENSP00000265104.4:n.5484+89_5484+91delinsTAA
NM_001369.2:c.5484+89_5484+91delinsTAA	NP_001360.1:n.5484+89_5484+91delinsTAA
XM_005248262.2:c.5439+89_5439+91delinsTAA	XP_005248319.1:n.5439+89_5439+91delinsTAA
XM_011513990.1:c.5484+89_5484+91delinsTAA	XP_011512292.1:n.5484+89_5484+91delinsTAA
XR_925598.1:n.5691+89_5691+91delinsTAA
XM_005248262.3:c.5592+89_5592+91delinsTAA	XP_005248319.2:n.5592+89_5592+91delinsTAA
XM_017009177.1:c.5592+89_5592+91delinsTAA	XP_016864666.1:n.5592+89_5592+91delinsTAA
XM_017009178.1:c.4497+89_4497+91delinsTAA	XP_016864667.1:n.4497+89_4497+91delinsTAA
XM_017009179.2:c.4497+89_4497+91delinsTAA	XP_016864668.1:n.4497+89_4497+91delinsTAA
XM_017009180.1:c.5592+89_5592+91delinsTAA	XP_016864669.1:n.5592+89_5592+91delinsTAA
XM_017009181.1:c.5592+89_5592+91delinsTAA	XP_016864670.1:n.5592+89_5592+91delinsTAA
XM_017009182.1:c.5592+89_5592+91delinsTAA	XP_016864671.1:n.5592+89_5592+91delinsTAA
XM_017009183.1:c.5592+89_5592+91delinsTAA	XP_016864672.1:n.5592+89_5592+91delinsTAA
XM_017009184.1:c.5592+89_5592+91delinsTAA	XP_016864673.1:n.5592+89_5592+91delinsTAA
XM_017009185.1:c.681+89_681+91delinsTAA	XP_016864674.1:n.681+89_681+91delinsTAA
XM_017009186.1:c.234+89_234+91delinsTAA	XP_016864675.1:n.234+89_234+91delinsTAA
XM_017009187.1:c.5592+89_5592+91delinsTAA	XP_016864676.1:n.5592+89_5592+91delinsTAA
XM_024454388.1:c.4497+89_4497+91delinsTAA	XP_024310156.1:n.4497+89_4497+91delinsTAA
XM_024454389.1:c.4086+89_4086+91delinsTAA	XP_024310157.1:n.4086+89_4086+91delinsTAA
XR_001742034.1:n.5609+89_5609+91delinsTAA
XR_001742035.1:n.5609+89_5609+91delinsTAA
NM_001369.3:c.5484+89_5484+91delinsTAA MANE Select	NP_001360.1:n.5484+89_5484+91delinsTAA