Canonical Allele Identifier: CA1528435513

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776780_13776782delinsCAG , CM000667.2:g.13776780_13776782delinsCAG	GRCh38
NC_000005.9:g.13776889_13776891delinsCAG , CM000667.1:g.13776889_13776891delinsCAG	GRCh37
NC_000005.8:g.13829889_13829891delinsCAG	NCBI36
NG_013081.1:g.172699_172701delinsCTG
NG_013081.2:g.172699_172701delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9106-76_9106-74delinsCTG MANE Select	ENSP00000265104.4:n.9106-76_9106-74delinsCTG
ENST00000681290.1:c.9061-76_9061-74delinsCTG	ENSP00000505288.1:n.9061-76_9061-74delinsCTG
ENST00000265104.4:c.9106-76_9106-74delinsCTG	ENSP00000265104.4:n.9106-76_9106-74delinsCTG
NM_001369.2:c.9106-76_9106-74delinsCTG	NP_001360.1:n.9106-76_9106-74delinsCTG
XM_005248262.2:c.9061-76_9061-74delinsCTG	XP_005248319.1:n.9061-76_9061-74delinsCTG
XM_011513990.1:c.9101-76_9101-74delinsCTG	XP_011512292.1:n.9101-76_9101-74delinsCTG
XR_925598.1:n.9177-76_9177-74delinsCTG
XM_005248262.3:c.9214-76_9214-74delinsCTG	XP_005248319.2:n.9214-76_9214-74delinsCTG
XM_017009177.1:c.9214-76_9214-74delinsCTG	XP_016864666.1:n.9214-76_9214-74delinsCTG
XM_017009178.1:c.8119-76_8119-74delinsCTG	XP_016864667.1:n.8119-76_8119-74delinsCTG
XM_017009179.2:c.8119-76_8119-74delinsCTG	XP_016864668.1:n.8119-76_8119-74delinsCTG
XM_017009180.1:c.9214-76_9214-74delinsCTG	XP_016864669.1:n.9214-76_9214-74delinsCTG
XM_017009181.1:c.9214-76_9214-74delinsCTG	XP_016864670.1:n.9214-76_9214-74delinsCTG
XM_017009182.1:c.9214-76_9214-74delinsCTG	XP_016864671.1:n.9214-76_9214-74delinsCTG
XM_017009183.1:c.9214-76_9214-74delinsCTG	XP_016864672.1:n.9214-76_9214-74delinsCTG
XM_017009184.1:c.9209-76_9209-74delinsCTG	XP_016864673.1:n.9209-76_9209-74delinsCTG
XM_017009185.1:c.4303-76_4303-74delinsCTG	XP_016864674.1:n.4303-76_4303-74delinsCTG
XM_017009186.1:c.3856-76_3856-74delinsCTG	XP_016864675.1:n.3856-76_3856-74delinsCTG
XM_017009188.1:c.3193-76_3193-74delinsCTG	XP_016864677.1:n.3193-76_3193-74delinsCTG
XM_024454388.1:c.8119-76_8119-74delinsCTG	XP_024310156.1:n.8119-76_8119-74delinsCTG
XM_024454389.1:c.7708-76_7708-74delinsCTG	XP_024310157.1:n.7708-76_7708-74delinsCTG
XR_001742034.1:n.9100-76_9100-74delinsCTG
XR_001742035.1:n.9095-76_9095-74delinsCTG
NM_001369.3:c.9106-76_9106-74delinsCTG MANE Select	NP_001360.1:n.9106-76_9106-74delinsCTG