Canonical Allele Identifier: CA1528441114
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13792474_13792475delinsCT , CM000667.2:g.13792474_13792475delinsCT GRCh38
NC_000005.9:g.13792583_13792584delinsCT , CM000667.1:g.13792583_13792584delinsCT GRCh37
NC_000005.8:g.13845583_13845584delinsCT NCBI36
NG_013081.1:g.157006_157007delinsAG
NG_013081.2:g.157006_157007delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.8225-258_8225-257delinsAG MANE Select ENSP00000265104.4:n.8225-258_8225-257delinsAG
ENST00000681290.1:c.8180-258_8180-257delinsAG ENSP00000505288.1:n.8180-258_8180-257delinsAG
ENST00000265104.4:c.8225-258_8225-257delinsAG ENSP00000265104.4:n.8225-258_8225-257delinsAG
NM_001369.2:c.8225-258_8225-257delinsAG NP_001360.1:n.8225-258_8225-257delinsAG
XM_005248262.2:c.8180-258_8180-257delinsAG XP_005248319.1:n.8180-258_8180-257delinsAG
XM_011513990.1:c.8225-258_8225-257delinsAG XP_011512292.1:n.8225-258_8225-257delinsAG
XR_925598.1:n.8432-258_8432-257delinsAG
XM_005248262.3:c.8333-258_8333-257delinsAG XP_005248319.2:n.8333-258_8333-257delinsAG
XM_017009177.1:c.8333-258_8333-257delinsAG XP_016864666.1:n.8333-258_8333-257delinsAG
XM_017009178.1:c.7238-258_7238-257delinsAG XP_016864667.1:n.7238-258_7238-257delinsAG
XM_017009179.2:c.7238-258_7238-257delinsAG XP_016864668.1:n.7238-258_7238-257delinsAG
XM_017009180.1:c.8333-258_8333-257delinsAG XP_016864669.1:n.8333-258_8333-257delinsAG
XM_017009181.1:c.8333-258_8333-257delinsAG XP_016864670.1:n.8333-258_8333-257delinsAG
XM_017009182.1:c.8333-258_8333-257delinsAG XP_016864671.1:n.8333-258_8333-257delinsAG
XM_017009183.1:c.8333-258_8333-257delinsAG XP_016864672.1:n.8333-258_8333-257delinsAG
XM_017009184.1:c.8333-258_8333-257delinsAG XP_016864673.1:n.8333-258_8333-257delinsAG
XM_017009185.1:c.3422-258_3422-257delinsAG XP_016864674.1:n.3422-258_3422-257delinsAG
XM_017009186.1:c.2975-258_2975-257delinsAG XP_016864675.1:n.2975-258_2975-257delinsAG
XM_017009188.1:c.2312-258_2312-257delinsAG XP_016864677.1:n.2312-258_2312-257delinsAG
XM_024454388.1:c.7238-258_7238-257delinsAG XP_024310156.1:n.7238-258_7238-257delinsAG
XM_024454389.1:c.6827-258_6827-257delinsAG XP_024310157.1:n.6827-258_6827-257delinsAG
XR_001742034.1:n.8350-258_8350-257delinsAG
XR_001742035.1:n.8350-258_8350-257delinsAG
NM_001369.3:c.8225-258_8225-257delinsAG MANE Select NP_001360.1:n.8225-258_8225-257delinsAG