Canonical Allele Identifier: CA1528435064

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13779552_13779553delinsTC , CM000667.2:g.13779552_13779553delinsTC	GRCh38
NC_000005.9:g.13779661_13779662delinsTC , CM000667.1:g.13779661_13779662delinsTC	GRCh37
NC_000005.8:g.13832661_13832662delinsTC	NCBI36
NG_013081.1:g.169928_169929delinsGA
NG_013081.2:g.169928_169929delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8951+1276_8951+1277delinsGA MANE Select	ENSP00000265104.4:n.8951+1276_8951+1277delinsGA
ENST00000681290.1:c.8906+1276_8906+1277delinsGA	ENSP00000505288.1:n.8906+1276_8906+1277delinsGA
ENST00000265104.4:c.8951+1276_8951+1277delinsGA	ENSP00000265104.4:n.8951+1276_8951+1277delinsGA
NM_001369.2:c.8951+1276_8951+1277delinsGA	NP_001360.1:n.8951+1276_8951+1277delinsGA
XM_005248262.2:c.8906+1276_8906+1277delinsGA	XP_005248319.1:n.8906+1276_8906+1277delinsGA
XM_011513990.1:c.8951+1276_8951+1277delinsGA	XP_011512292.1:n.8951+1276_8951+1277delinsGA
XR_925598.1:n.9028-2198_9028-2197delinsGA
XM_005248262.3:c.9059+1276_9059+1277delinsGA	XP_005248319.2:n.9059+1276_9059+1277delinsGA
XM_017009177.1:c.9059+1276_9059+1277delinsGA	XP_016864666.1:n.9059+1276_9059+1277delinsGA
XM_017009178.1:c.7964+1276_7964+1277delinsGA	XP_016864667.1:n.7964+1276_7964+1277delinsGA
XM_017009179.2:c.7964+1276_7964+1277delinsGA	XP_016864668.1:n.7964+1276_7964+1277delinsGA
XM_017009180.1:c.9059+1276_9059+1277delinsGA	XP_016864669.1:n.9059+1276_9059+1277delinsGA
XM_017009181.1:c.9059+1276_9059+1277delinsGA	XP_016864670.1:n.9059+1276_9059+1277delinsGA
XM_017009182.1:c.9059+1276_9059+1277delinsGA	XP_016864671.1:n.9059+1276_9059+1277delinsGA
XM_017009183.1:c.9059+1276_9059+1277delinsGA	XP_016864672.1:n.9059+1276_9059+1277delinsGA
XM_017009184.1:c.9059+1276_9059+1277delinsGA	XP_016864673.1:n.9059+1276_9059+1277delinsGA
XM_017009185.1:c.4148+1276_4148+1277delinsGA	XP_016864674.1:n.4148+1276_4148+1277delinsGA
XM_017009186.1:c.3701+1276_3701+1277delinsGA	XP_016864675.1:n.3701+1276_3701+1277delinsGA
XM_017009188.1:c.3038+1276_3038+1277delinsGA	XP_016864677.1:n.3038+1276_3038+1277delinsGA
XM_024454388.1:c.7964+1276_7964+1277delinsGA	XP_024310156.1:n.7964+1276_7964+1277delinsGA
XM_024454389.1:c.7553+1276_7553+1277delinsGA	XP_024310157.1:n.7553+1276_7553+1277delinsGA
XR_001742034.1:n.8946-2198_8946-2197delinsGA
XR_001742035.1:n.8946-2198_8946-2197delinsGA
NM_001369.3:c.8951+1276_8951+1277delinsGA MANE Select	NP_001360.1:n.8951+1276_8951+1277delinsGA