Canonical Allele Identifier: CA1528476607

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13871035_13871036delinsTA , CM000667.2:g.13871035_13871036delinsTA	GRCh38
NC_000005.9:g.13871144_13871145delinsTA , CM000667.1:g.13871144_13871145delinsTA	GRCh37
NC_000005.8:g.13924144_13924145delinsTA	NCBI36
NG_013081.1:g.78445_78446delinsTA
NG_013081.2:g.78445_78446delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.3599-34_3599-33delinsTA MANE Select	ENSP00000265104.4:n.3599-34_3599-33delinsTA
ENST00000681290.1:c.3554-34_3554-33delinsTA	ENSP00000505288.1:n.3554-34_3554-33delinsTA
ENST00000265104.4:c.3599-34_3599-33delinsTA	ENSP00000265104.4:n.3599-34_3599-33delinsTA
NM_001369.2:c.3599-34_3599-33delinsTA	NP_001360.1:n.3599-34_3599-33delinsTA
XM_005248262.2:c.3554-34_3554-33delinsTA	XP_005248319.1:n.3554-34_3554-33delinsTA
XM_011513990.1:c.3599-34_3599-33delinsTA	XP_011512292.1:n.3599-34_3599-33delinsTA
XR_925598.1:n.3806-34_3806-33delinsTA
XM_005248262.3:c.3707-34_3707-33delinsTA	XP_005248319.2:n.3707-34_3707-33delinsTA
XM_017009177.1:c.3707-34_3707-33delinsTA	XP_016864666.1:n.3707-34_3707-33delinsTA
XM_017009178.1:c.2612-34_2612-33delinsTA	XP_016864667.1:n.2612-34_2612-33delinsTA
XM_017009179.2:c.2612-34_2612-33delinsTA	XP_016864668.1:n.2612-34_2612-33delinsTA
XM_017009180.1:c.3707-34_3707-33delinsTA	XP_016864669.1:n.3707-34_3707-33delinsTA
XM_017009181.1:c.3707-34_3707-33delinsTA	XP_016864670.1:n.3707-34_3707-33delinsTA
XM_017009182.1:c.3707-34_3707-33delinsTA	XP_016864671.1:n.3707-34_3707-33delinsTA
XM_017009183.1:c.3707-34_3707-33delinsTA	XP_016864672.1:n.3707-34_3707-33delinsTA
XM_017009184.1:c.3707-34_3707-33delinsTA	XP_016864673.1:n.3707-34_3707-33delinsTA
XM_017009187.1:c.3707-34_3707-33delinsTA	XP_016864676.1:n.3707-34_3707-33delinsTA
XM_024454388.1:c.2612-34_2612-33delinsTA	XP_024310156.1:n.2612-34_2612-33delinsTA
XM_024454389.1:c.2201-34_2201-33delinsTA	XP_024310157.1:n.2201-34_2201-33delinsTA
XR_001742034.1:n.3724-34_3724-33delinsTA
XR_001742035.1:n.3724-34_3724-33delinsTA
NM_001369.3:c.3599-34_3599-33delinsTA MANE Select	NP_001360.1:n.3599-34_3599-33delinsTA