Canonical Allele Identifier: CA1528435575

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776861_13776865delinsAAAAT , CM000667.2:g.13776861_13776865delinsAAAAT	GRCh38
NC_000005.9:g.13776970_13776974delinsAAAAT , CM000667.1:g.13776970_13776974delinsAAAAT	GRCh37
NC_000005.8:g.13829970_13829974delinsAAAAT	NCBI36
NG_013081.1:g.172616_172620delinsATTTT
NG_013081.2:g.172616_172620delinsATTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9106-159_9106-155delinsATTTT MANE Select	ENSP00000265104.4:n.9106-159_9106-155delinsATTTT
ENST00000681290.1:c.9061-159_9061-155delinsATTTT	ENSP00000505288.1:n.9061-159_9061-155delinsATTTT
ENST00000265104.4:c.9106-159_9106-155delinsATTTT	ENSP00000265104.4:n.9106-159_9106-155delinsATTTT
NM_001369.2:c.9106-159_9106-155delinsATTTT	NP_001360.1:n.9106-159_9106-155delinsATTTT
XM_005248262.2:c.9061-159_9061-155delinsATTTT	XP_005248319.1:n.9061-159_9061-155delinsATTTT
XM_011513990.1:c.9101-159_9101-155delinsATTTT	XP_011512292.1:n.9101-159_9101-155delinsATTTT
XR_925598.1:n.9177-159_9177-155delinsATTTT
XM_005248262.3:c.9214-159_9214-155delinsATTTT	XP_005248319.2:n.9214-159_9214-155delinsATTTT
XM_017009177.1:c.9214-159_9214-155delinsATTTT	XP_016864666.1:n.9214-159_9214-155delinsATTTT
XM_017009178.1:c.8119-159_8119-155delinsATTTT	XP_016864667.1:n.8119-159_8119-155delinsATTTT
XM_017009179.2:c.8119-159_8119-155delinsATTTT	XP_016864668.1:n.8119-159_8119-155delinsATTTT
XM_017009180.1:c.9214-159_9214-155delinsATTTT	XP_016864669.1:n.9214-159_9214-155delinsATTTT
XM_017009181.1:c.9214-159_9214-155delinsATTTT	XP_016864670.1:n.9214-159_9214-155delinsATTTT
XM_017009182.1:c.9214-159_9214-155delinsATTTT	XP_016864671.1:n.9214-159_9214-155delinsATTTT
XM_017009183.1:c.9214-159_9214-155delinsATTTT	XP_016864672.1:n.9214-159_9214-155delinsATTTT
XM_017009184.1:c.9209-159_9209-155delinsATTTT	XP_016864673.1:n.9209-159_9209-155delinsATTTT
XM_017009185.1:c.4303-159_4303-155delinsATTTT	XP_016864674.1:n.4303-159_4303-155delinsATTTT
XM_017009186.1:c.3856-159_3856-155delinsATTTT	XP_016864675.1:n.3856-159_3856-155delinsATTTT
XM_017009188.1:c.3193-159_3193-155delinsATTTT	XP_016864677.1:n.3193-159_3193-155delinsATTTT
XM_024454388.1:c.8119-159_8119-155delinsATTTT	XP_024310156.1:n.8119-159_8119-155delinsATTTT
XM_024454389.1:c.7708-159_7708-155delinsATTTT	XP_024310157.1:n.7708-159_7708-155delinsATTTT
XR_001742034.1:n.9100-159_9100-155delinsATTTT
XR_001742035.1:n.9095-159_9095-155delinsATTTT
NM_001369.3:c.9106-159_9106-155delinsATTTT MANE Select	NP_001360.1:n.9106-159_9106-155delinsATTTT