Canonical Allele Identifier: CA1528399842

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13701205_13701211delinsAGTCTTT , CM000667.2:g.13701205_13701211delinsAGTCTTT	GRCh38
NC_000005.9:g.13701314_13701320delinsAGTCTTT , CM000667.1:g.13701314_13701320delinsAGTCTTT	GRCh37
NC_000005.8:g.13754314_13754320delinsAGTCTTT	NCBI36
NG_013081.1:g.248270_248276delinsAAAGACT
NG_013081.2:g.248270_248276delinsAAAGACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.824+73_824+79delinsAAAGACT
ENST00000265104.5:c.13491+73_13491+79delinsAAAGACT MANE Select	ENSP00000265104.4:n.13491+73_13491+79delinsAAAGACT
ENST00000681290.1:c.13446+73_13446+79delinsAAAGACT	ENSP00000505288.1:n.13446+73_13446+79delinsAAAGACT
ENST00000265104.4:c.13491+73_13491+79delinsAAAGACT	ENSP00000265104.4:n.13491+73_13491+79delinsAAAGACT
NM_001369.2:c.13491+73_13491+79delinsAAAGACT	NP_001360.1:n.13491+73_13491+79delinsAAAGACT
XM_005248262.2:c.13446+73_13446+79delinsAAAGACT	XP_005248319.1:n.13446+73_13446+79delinsAAAGACT
XM_005248262.3:c.13599+73_13599+79delinsAAAGACT	XP_005248319.2:n.13599+73_13599+79delinsAAAGACT
XM_017009177.1:c.13179+73_13179+79delinsAAAGACT	XP_016864666.1:n.13179+73_13179+79delinsAAAGACT
XM_017009178.1:c.12504+73_12504+79delinsAAAGACT	XP_016864667.1:n.12504+73_12504+79delinsAAAGACT
XM_017009179.2:c.12504+73_12504+79delinsAAAGACT	XP_016864668.1:n.12504+73_12504+79delinsAAAGACT
XM_017009185.1:c.8688+73_8688+79delinsAAAGACT	XP_016864674.1:n.8688+73_8688+79delinsAAAGACT
XM_017009186.1:c.8241+73_8241+79delinsAAAGACT	XP_016864675.1:n.8241+73_8241+79delinsAAAGACT
XM_017009188.1:c.7578+73_7578+79delinsAAAGACT	XP_016864677.1:n.7578+73_7578+79delinsAAAGACT
XM_024454388.1:c.12504+73_12504+79delinsAAAGACT	XP_024310156.1:n.12504+73_12504+79delinsAAAGACT
XM_024454389.1:c.12093+73_12093+79delinsAAAGACT	XP_024310157.1:n.12093+73_12093+79delinsAAAGACT
NM_001369.3:c.13491+73_13491+79delinsAAAGACT MANE Select	NP_001360.1:n.13491+73_13491+79delinsAAAGACT